|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Jun 14th, 2020 12:00AM
|
Director, Program Management - Contract
|
Open
|
Program Management
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jun 11th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides or ERSGs) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons have been identified in over 1,800 rare and ultra-rare diseases.
<p>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx’s preclinical candidate pool consists of a library of novel drug candidates designed to be ERSGs identified based on read-through potential. Eloxx also has preclinical programs focused on rare ocular genetic disorders and polycystic kidney disease.</p>
<p>Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ. For more information, please visit <u>www.eloxxpharma.com</u>.</p>
</div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>Eloxx Pharmaceuticals is looking for Director of Program Management -Contractor to lead cross-functional projects in a fast-paced environment. The expected contract will be 5 – 6 months with the possibility to extend. This roles will be responsible for maintaining, integrating and executing plans, schedules and budgets for all of Eloxx’s disease areas. This is a highly visible role, working closely with the CEO to make a big impact on the success of our program teams while our Lead Program Manager is on maternity leave. </div>
<div class="generic-details-text"> </div>
<div class="generic-details-text">This position is based in our Waltham, MA Headquarters although remote work is currently an option.</div>
<div class="generic-details-text"><br><br><strong>Responsibilities:<br></strong>
<ul>
<li>Maintain study tracking tools, decision logs and study calendars to ensure deadlines and deliverables are met on or ahead of schedule</li>
<li>Compile budgets and track actual expenditures</li>
<li>Meet with functional heads regularly to capture progress updates on individual tasks and ensure sub-team timelines are aligned with overall project timelines across multiple programs</li>
<li>Coordinate core team meetings, including setting agendas, capturing meeting minutes, and ensuring appropriate follow-up for action items.</li>
<li>Identify and anticipate challenges, assist in developing risk assessment and mitigation plans by working closely with cross-functional team leads and appropriately elevating issues in a timely manner</li>
<li>Serve as lead CMC Project Manager responsible for monitoring and directing work, tracking and approving invoices, and managing material inventory and distribution of materials per program plans</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Excellent communication and interpersonal skills</li>
<li>Aptitude for organizational detail and ability to manage multiple projects</li>
<li>Ability to interact across all levels of the organization</li>
<li>Capacity to complete tasks independently in a highly-regulated environment</li>
<li>Flexibility to function well within a team environment and within condensed timelines</li>
<li>Ability to verbalize complex study issues and demonstrated problem-solving ability</li>
</ul>
<strong><br>Experience/Education:</strong>
<ul>
<li>B.S. in a relevant field with 5+ years of direct Project/Program Management experience in the pharmaceutical or biotechnology industry, CMC experience is preferred but not required</li>
<li>PMP Certification preferred</li>
<li>Experience overseeing and coordinating with consultants/vendors</li>
<li>Experience tracking task completion, working with various functional areas to drive timelines and identify/escalate issues and risks</li>
<li>Experience leading cross-functional team meetings</li>
<li>Experience with related software is a plus but is not required: smartsheets, MS project, MS Timeline, OneNote, SharePoint</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
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|
|
|
|
Jun 14th, 2020 01:14PM
|
Jun 14th, 2020 01:14PM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Aug 24th, 2020 12:00AM
|
Toxicology/DMPK, Senior Scientist
|
Open
|
Pharmacology
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jul 29th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides or ERSGs) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons have been identified in over 1,800 rare and ultra-rare diseases.
<p>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx’s preclinical candidate pool consists of a library of novel drug candidates designed to be ERSGs identified based on read-through potential. Eloxx also has preclinical programs focused on rare ocular genetic disorders and polycystic kidney disease.</p>
<p>Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ. &nbsp;For more information, please visit <u>www.eloxxpharma.com</u>.</p>
&nbsp;</div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>The Senior Scientist Toxicology is responsible for timely and effective drug safety and/or pharmacokinetic support for preclinical programs. The incumbent is expected to demonstrate competency in interpreting toxicology/ drug metabolism and pharmacokinetics (DMPK)&nbsp;data, development and implementation of strategic plans for pre- and non-clinical development, as well as providing expertise and guidance in Toxicology/DMPK to project and program teams.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text">This individual will be highly analytical, decisive, goal-oriented, and timeline sensitive while maintaining the highest of scientific and ethical standards. Reporting to the Vice President of Research, the Senior Scientist Toxicology will actively participate on project/program/product teams, as well as collaborate with research leadership on reviewing new business initiatives and opportunities.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><br><strong>Responsibilities:<br></strong></div>
<div class="generic-details-text">
<ul>
<li>Review and approve Toxicology/DMPK study protocols, reports, associated data.</li>
<li>Nonclinical summaries, Regulatory submission sections and associated documentation.</li>
<li>Design, manage, analyze, review, summarize, interpret and report results of Toxicology, Safety Pharmacology and DMPK studies generated through partner CROs.</li>
<li>Maintain up-to-date Toxicology and/or DMPK plans (linked to overall program plans) for all projects/programs/products, including listings of studies, timelines, status and costs; update and refine as necessary.</li>
<li>Provide scientific/technical due diligence support for Business Development activities as required.</li>
<li>Assist in preparation for regulatory agency interactions.</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Qualifications:</strong></div>
<div class="generic-details-text">
<ul>
<li>Demonstrated knowledge of global regulatory requirements and expectations for nonclinical safety assessment packages to support first in human studies, including thorough knowledge of GLP, GCP, ICH and other applicable global guidelines.</li>
<li>Extensive experience in the outsourcing and external oversight of nonclinical Toxicology/DMPK studies conducted by qualified suppliers.</li>
<li>Hands-on experience in Toxicology and/or DMPK study conduct including general, genetic, developmental and reproductive toxicology, carcinogenicity, toxicokinetics, ADME and safety pharmacology.</li>
<li>Experience representing function to global regulatory agencies in support of IND/CTA submissions.</li>
</ul>
</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Ability to define problems, design experiments, analyze and interpret results.</li>
<li>Ability to prioritize responsibilities and meet deadlines.</li>
<li>Ability to self-motivate and work independently.</li>
<li>Strong attention to detail, experience in monitoring work to assure quality, accuracy and thoroughness.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Demonstrated ability to work on complex problems and business processes in which the analysis of situations and/or data frequently requires an in-depth evaluation of multiple, interdependent factors and professional judgment.</li>
<li>Excellent communication skills with an ability to communicate across a variety of audiences including team members, cross-functional project teams, leaders, vendors and senior management.</li>
<li>Ability to work at the strategic and tactical level.</li>
<li>Enthusiastic, positive, upbeat “can do” attitude; doesn’t take themselves too seriously, has a sense of humor and is a team player.</li>
<li>The ability to work well in a fast paced, innovative and performance driven environment.</li>
<li></li>
</ul>
<strong>Experience/Education:</strong>
<ul>
<li>PhD in a related subject, with DABT certification preferred, but not required.</li>
<li>3+ years industry-related experience in regulatory Toxicology and DMPK working within Biotech and pharmaceutical industry.</li>
<li>Experience with both small and macromolecular/biologic drugs is highly desirable.</li>
<li>Experience in providing formal scientific/technical due diligence support for Business Development.</li>
<li>Experience in Investigative Toxicology and preclinical development of ophthalmology, pulmonary or Gene Therapy drugs is highly desirable.</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
|
|
|
|
|
Aug 24th, 2020 10:08AM
|
Aug 24th, 2020 10:08AM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Aug 16th, 2020 12:00AM
|
Toxicology/DMPK, Senior Scientist
|
Open
|
Pharmacology
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jul 29th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides or ERSGs) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons have been identified in over 1,800 rare and ultra-rare diseases.
<p>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx’s preclinical candidate pool consists of a library of novel drug candidates designed to be ERSGs identified based on read-through potential. Eloxx also has preclinical programs focused on rare ocular genetic disorders and polycystic kidney disease.</p>
<p>Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ. &nbsp;For more information, please visit <u>www.eloxxpharma.com</u>.</p>
&nbsp;</div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>The Senior Scientist Toxicology is responsible for timely and effective drug safety and/or pharmacokinetic support for preclinical programs. The incumbent is expected to demonstrate competency in interpreting toxicology/ drug metabolism and pharmacokinetics (DMPK)&nbsp;data, development and implementation of strategic plans for pre- and non-clinical development, as well as providing expertise and guidance in Toxicology/DMPK to project and program teams.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text">This individual will be highly analytical, decisive, goal-oriented, and timeline sensitive while maintaining the highest of scientific and ethical standards. Reporting to the Vice President of Research, the Senior Scientist Toxicology will actively participate on project/program/product teams, as well as collaborate with research leadership on reviewing new business initiatives and opportunities.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><br><strong>Responsibilities:<br></strong></div>
<div class="generic-details-text">
<ul>
<li>Review and approve Toxicology/DMPK study protocols, reports, associated data.</li>
<li>Nonclinical summaries, Regulatory submission sections and associated documentation.</li>
<li>Design, manage, analyze, review, summarize, interpret and report results of Toxicology, Safety Pharmacology and DMPK studies generated through partner CROs.</li>
<li>Maintain up-to-date Toxicology and/or DMPK plans (linked to overall program plans) for all projects/programs/products, including listings of studies, timelines, status and costs; update and refine as necessary.</li>
<li>Provide scientific/technical due diligence support for Business Development activities as required.</li>
<li>Assist in preparation for regulatory agency interactions.</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Qualifications:</strong></div>
<div class="generic-details-text">
<ul>
<li>Demonstrated knowledge of global regulatory requirements and expectations for nonclinical safety assessment packages to support first in human studies, including thorough knowledge of GLP, GCP, ICH and other applicable global guidelines.</li>
<li>Extensive experience in the outsourcing and external oversight of nonclinical Toxicology/DMPK studies conducted by qualified suppliers.</li>
<li>Hands-on experience in Toxicology and/or DMPK study conduct including general, genetic, developmental and reproductive toxicology, carcinogenicity, toxicokinetics, ADME and safety pharmacology.</li>
<li>Experience representing function to global regulatory agencies in support of IND/CTA submissions.</li>
</ul>
</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Ability to define problems, design experiments, analyze and interpret results.</li>
<li>Ability to prioritize responsibilities and meet deadlines.</li>
<li>Ability to self-motivate and work independently.</li>
<li>Strong attention to detail, experience in monitoring work to assure quality, accuracy and thoroughness.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Demonstrated ability to work on complex problems and business processes in which the analysis of situations and/or data frequently requires an in-depth evaluation of multiple, interdependent factors and professional judgment.</li>
<li>Excellent communication skills with an ability to communicate across a variety of audiences including team members, cross-functional project teams, leaders, vendors and senior management.</li>
<li>Ability to work at the strategic and tactical level.</li>
<li>Enthusiastic, positive, upbeat “can do” attitude; doesn’t take themselves too seriously, has a sense of humor and is a team player.</li>
<li>The ability to work well in a fast paced, innovative and performance driven environment.</li>
<li></li>
</ul>
<strong>Experience/Education:</strong>
<ul>
<li>PhD in a related subject, with DABT certification preferred, but not required.</li>
<li>3+ years industry-related experience in regulatory Toxicology and DMPK working within Biotech and pharmaceutical industry.</li>
<li>Experience with both small and macromolecular/biologic drugs is highly desirable.</li>
<li>Experience in providing formal scientific/technical due diligence support for Business Development.</li>
<li>Experience in Investigative Toxicology and preclinical development of ophthalmology, pulmonary or Gene Therapy drugs is highly desirable.</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
|
|
|
|
|
Aug 16th, 2020 07:19PM
|
Aug 16th, 2020 07:19PM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Jun 21st, 2020 12:00AM
|
Contract Program Manager
|
Open
|
Program Management
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jun 11th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides or ERSGs) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons have been identified in over 1,800 rare and ultra-rare diseases.
<p>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx’s preclinical candidate pool consists of a library of novel drug candidates designed to be ERSGs identified based on read-through potential. Eloxx also has preclinical programs focused on rare ocular genetic disorders and polycystic kidney disease.</p>
<p>Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ. For more information, please visit <u>www.eloxxpharma.com</u>.</p>
</div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>Eloxx Pharmaceuticals is looking for a Contract Program Manager to lead cross-functional projects in a fast-paced environment. The Contract Program Manager maintains, integrates and executes plans, schedules and budgets for all of Eloxx’s disease areas. This is a highly visible role, working closely with the CEO to make a big impact on the success of our program teams while our Lead Program Manager is on maternity leave. The expected contract will be 5 – 6 months with the possibility to extend.<strong><strong><br></strong></strong> </div>
<div class="generic-details-text">This position is based in our Waltham, MA Headquarters although remote work is currently an option.</div>
<div class="generic-details-text"><br><br><strong>Responsibilities:<br></strong>
<ul>
<li>Maintain study tracking tools, decision logs and study calendars to ensure deadlines and deliverables are met on or ahead of schedule</li>
<li>Compile budgets and track actual expenditures</li>
<li>Meet with functional heads regularly to capture progress updates on individual tasks and ensure sub-team timelines are aligned with overall project timelines across multiple programs</li>
<li>Coordinate core team meetings, including setting agendas, capturing meeting minutes, and ensuring appropriate follow-up for action items.</li>
<li>Identify and anticipate challenges, assist in developing risk assessment and mitigation plans by working closely with cross-functional team leads and appropriately elevating issues in a timely manner</li>
<li>Serve as lead CMC Project Manager responsible for monitoring and directing work, tracking and approving invoices, and managing material inventory and distribution of materials per program plans</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Excellent communication and interpersonal skills</li>
<li>Aptitude for organizational detail and ability to manage multiple projects</li>
<li>Ability to interact across all levels of the organization</li>
<li>Capacity to complete tasks independently in a highly-regulated environment</li>
<li>Flexibility to function well within a team environment and within condensed timelines</li>
<li>Ability to verbalize complex study issues and demonstrated problem-solving ability</li>
</ul>
<strong><br>Experience/Education:</strong>
<ul>
<li>B.S. in a relevant field with 5+ years of direct Project/Program Management experience in the pharmaceutical or biotechnology industry, CMC experience is preferred but not required</li>
<li>PMP Certification preferred</li>
<li>Experience overseeing and coordinating with consultants/vendors</li>
<li>Experience tracking task completion, working with various functional areas to drive timelines and identify/escalate issues and risks</li>
<li>Experience leading cross-functional team meetings</li>
<li>Experience with related software is a plus but is not required: smartsheets, MS project, MS Timeline, OneNote, SharePoint</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
|
|
|
|
|
Jun 21st, 2020 03:33PM
|
Jun 21st, 2020 03:33PM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Jul 1st, 2020 12:00AM
|
Director, Program Management - Contract
|
Open
|
Program Management
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jun 11th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides or ERSGs) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons have been identified in over 1,800 rare and ultra-rare diseases.
<p>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx’s preclinical candidate pool consists of a library of novel drug candidates designed to be ERSGs identified based on read-through potential. Eloxx also has preclinical programs focused on rare ocular genetic disorders and polycystic kidney disease.</p>
<p>Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ. For more information, please visit <u>www.eloxxpharma.com</u>.</p>
</div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>Eloxx Pharmaceuticals is looking for Director of Program Management -Contractor to lead cross-functional projects in a fast-paced environment. The expected contract will be 5 – 6 months with the possibility to extend. This roles will be responsible for maintaining, integrating and executing plans, schedules and budgets for all of Eloxx’s disease areas. This is a highly visible role, working closely with the CEO to make a big impact on the success of our program teams while our Lead Program Manager is on maternity leave. </div>
<div class="generic-details-text"> </div>
<div class="generic-details-text">This position is based in our Waltham, MA Headquarters although remote work is currently an option.</div>
<div class="generic-details-text"><br><br><strong>Responsibilities:<br></strong>
<ul>
<li>Maintain study tracking tools, decision logs and study calendars to ensure deadlines and deliverables are met on or ahead of schedule</li>
<li>Compile budgets and track actual expenditures</li>
<li>Meet with functional heads regularly to capture progress updates on individual tasks and ensure sub-team timelines are aligned with overall project timelines across multiple programs</li>
<li>Coordinate core team meetings, including setting agendas, capturing meeting minutes, and ensuring appropriate follow-up for action items.</li>
<li>Identify and anticipate challenges, assist in developing risk assessment and mitigation plans by working closely with cross-functional team leads and appropriately elevating issues in a timely manner</li>
<li>Serve as lead CMC Project Manager responsible for monitoring and directing work, tracking and approving invoices, and managing material inventory and distribution of materials per program plans</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Excellent communication and interpersonal skills</li>
<li>Aptitude for organizational detail and ability to manage multiple projects</li>
<li>Ability to interact across all levels of the organization</li>
<li>Capacity to complete tasks independently in a highly-regulated environment</li>
<li>Flexibility to function well within a team environment and within condensed timelines</li>
<li>Ability to verbalize complex study issues and demonstrated problem-solving ability</li>
</ul>
<strong><br>Experience/Education:</strong>
<ul>
<li>B.S. in a relevant field with 5+ years of direct Project/Program Management experience in the pharmaceutical or biotechnology industry, CMC experience is preferred but not required</li>
<li>PMP Certification preferred</li>
<li>Experience overseeing and coordinating with consultants/vendors</li>
<li>Experience tracking task completion, working with various functional areas to drive timelines and identify/escalate issues and risks</li>
<li>Experience leading cross-functional team meetings</li>
<li>Experience with related software is a plus but is not required: smartsheets, MS project, MS Timeline, OneNote, SharePoint</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
|
|
|
|
|
Jul 1st, 2020 02:51PM
|
Jul 1st, 2020 02:51PM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Jul 17th, 2020 12:00AM
|
Toxicology/DMPK, Senior Scientist
|
Open
|
Pharmacology
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jul 10th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides or ERSGs) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons have been identified in over 1,800 rare and ultra-rare diseases.
<p>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx’s preclinical candidate pool consists of a library of novel drug candidates designed to be ERSGs identified based on read-through potential. Eloxx also has preclinical programs focused on rare ocular genetic disorders and polycystic kidney disease.</p>
<p>Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ. &nbsp;For more information, please visit <u>www.eloxxpharma.com</u>.</p>
&nbsp;</div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>The Senior Scientist Toxicology is responsible for timely and effective drug safety and/or pharmacokinetic support for preclinical programs. The incumbent is expected to demonstrate competency in interpreting toxicology/ drug metabolism and pharmacokinetics (DMPK)&nbsp;data, development and implementation of strategic plans for pre- and non-clinical development, as well as providing expertise and guidance in Toxicology/DMPK to project and program teams.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text">This individual will be highly analytical, decisive, goal-oriented, and timeline sensitive while maintaining the highest of scientific and ethical standards. Reporting to the Vice President of Research, the Senior Scientist Toxicology will actively participate on project/program/product teams, as well as collaborate with research leadership on reviewing new business initiatives and opportunities.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><br><strong>Responsibilities:<br></strong></div>
<div class="generic-details-text">
<ul>
<li>Review and approve Toxicology/DMPK study protocols, reports, associated data.</li>
<li>Nonclinical summaries, Regulatory submission sections and associated documentation.</li>
<li>Design, manage, analyze, review, summarize, interpret and report results of Toxicology, Safety Pharmacology and DMPK studies generated through partner CROs.</li>
<li>Maintain up-to-date Toxicology and/or DMPK plans (linked to overall program plans) for all projects/programs/products, including listings of studies, timelines, status and costs; update and refine as necessary.</li>
<li>Provide scientific/technical due diligence support for Business Development activities as required.</li>
<li>Assist in preparation for regulatory agency interactions.</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Qualifications:</strong></div>
<div class="generic-details-text">
<ul>
<li>Demonstrated knowledge of global regulatory requirements and expectations for nonclinical safety assessment packages to support first in human studies, including thorough knowledge of GLP, GCP, ICH and other applicable global guidelines.</li>
<li>Extensive experience in the outsourcing and external oversight of nonclinical Toxicology/DMPK studies conducted by qualified suppliers.</li>
<li>Hands-on experience in Toxicology and/or DMPK study conduct including general, genetic, developmental and reproductive toxicology, carcinogenicity, toxicokinetics, ADME and safety pharmacology.</li>
<li>Experience representing function to global regulatory agencies in support of IND/CTA submissions.</li>
</ul>
</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Ability to define problems, design experiments, analyze and interpret results.</li>
<li>Ability to prioritize responsibilities and meet deadlines.</li>
<li>Ability to self-motivate and work independently.</li>
<li>Strong attention to detail, experience in monitoring work to assure quality, accuracy and thoroughness.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Demonstrated ability to work on complex problems and business processes in which the analysis of situations and/or data frequently requires an in-depth evaluation of multiple, interdependent factors and professional judgment.</li>
<li>Excellent communication skills with an ability to communicate across a variety of audiences including team members, cross-functional project teams, leaders, vendors and senior management.</li>
<li>Ability to work at the strategic and tactical level.</li>
<li>Enthusiastic, positive, upbeat “can do” attitude; doesn’t take themselves too seriously, has a sense of humor and is a team player.</li>
<li>The ability to work well in a fast paced, innovative and performance driven environment.</li>
<li></li>
</ul>
<strong>Experience/Education:</strong>
<ul>
<li>PhD in a related subject, with DABT certification preferred, but not required.</li>
<li>3+ years industry-related experience in regulatory Toxicology and DMPK working within Biotech and pharmaceutical industry.</li>
<li>Experience with both small and macromolecular/biologic drugs is highly desirable.</li>
<li>Experience in providing formal scientific/technical due diligence support for Business Development.</li>
<li>Experience in Investigative Toxicology and preclinical development of ophthalmology, pulmonary or Gene Therapy drugs is highly desirable.</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
|
|
|
|
|
Jul 17th, 2020 03:33PM
|
Jul 17th, 2020 03:33PM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Jul 20th, 2020 12:00AM
|
Toxicology/DMPK, Senior Scientist
|
Open
|
Pharmacology
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jul 10th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides or ERSGs) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons have been identified in over 1,800 rare and ultra-rare diseases.
<p>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx’s preclinical candidate pool consists of a library of novel drug candidates designed to be ERSGs identified based on read-through potential. Eloxx also has preclinical programs focused on rare ocular genetic disorders and polycystic kidney disease.</p>
<p>Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ. &nbsp;For more information, please visit <u>www.eloxxpharma.com</u>.</p>
&nbsp;</div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>The Senior Scientist Toxicology is responsible for timely and effective drug safety and/or pharmacokinetic support for preclinical programs. The incumbent is expected to demonstrate competency in interpreting toxicology/ drug metabolism and pharmacokinetics (DMPK)&nbsp;data, development and implementation of strategic plans for pre- and non-clinical development, as well as providing expertise and guidance in Toxicology/DMPK to project and program teams.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text">This individual will be highly analytical, decisive, goal-oriented, and timeline sensitive while maintaining the highest of scientific and ethical standards. Reporting to the Vice President of Research, the Senior Scientist Toxicology will actively participate on project/program/product teams, as well as collaborate with research leadership on reviewing new business initiatives and opportunities.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><br><strong>Responsibilities:<br></strong></div>
<div class="generic-details-text">
<ul>
<li>Review and approve Toxicology/DMPK study protocols, reports, associated data.</li>
<li>Nonclinical summaries, Regulatory submission sections and associated documentation.</li>
<li>Design, manage, analyze, review, summarize, interpret and report results of Toxicology, Safety Pharmacology and DMPK studies generated through partner CROs.</li>
<li>Maintain up-to-date Toxicology and/or DMPK plans (linked to overall program plans) for all projects/programs/products, including listings of studies, timelines, status and costs; update and refine as necessary.</li>
<li>Provide scientific/technical due diligence support for Business Development activities as required.</li>
<li>Assist in preparation for regulatory agency interactions.</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Qualifications:</strong></div>
<div class="generic-details-text">
<ul>
<li>Demonstrated knowledge of global regulatory requirements and expectations for nonclinical safety assessment packages to support first in human studies, including thorough knowledge of GLP, GCP, ICH and other applicable global guidelines.</li>
<li>Extensive experience in the outsourcing and external oversight of nonclinical Toxicology/DMPK studies conducted by qualified suppliers.</li>
<li>Hands-on experience in Toxicology and/or DMPK study conduct including general, genetic, developmental and reproductive toxicology, carcinogenicity, toxicokinetics, ADME and safety pharmacology.</li>
<li>Experience representing function to global regulatory agencies in support of IND/CTA submissions.</li>
</ul>
</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Ability to define problems, design experiments, analyze and interpret results.</li>
<li>Ability to prioritize responsibilities and meet deadlines.</li>
<li>Ability to self-motivate and work independently.</li>
<li>Strong attention to detail, experience in monitoring work to assure quality, accuracy and thoroughness.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Demonstrated ability to work on complex problems and business processes in which the analysis of situations and/or data frequently requires an in-depth evaluation of multiple, interdependent factors and professional judgment.</li>
<li>Excellent communication skills with an ability to communicate across a variety of audiences including team members, cross-functional project teams, leaders, vendors and senior management.</li>
<li>Ability to work at the strategic and tactical level.</li>
<li>Enthusiastic, positive, upbeat “can do” attitude; doesn’t take themselves too seriously, has a sense of humor and is a team player.</li>
<li>The ability to work well in a fast paced, innovative and performance driven environment.</li>
<li></li>
</ul>
<strong>Experience/Education:</strong>
<ul>
<li>PhD in a related subject, with DABT certification preferred, but not required.</li>
<li>3+ years industry-related experience in regulatory Toxicology and DMPK working within Biotech and pharmaceutical industry.</li>
<li>Experience with both small and macromolecular/biologic drugs is highly desirable.</li>
<li>Experience in providing formal scientific/technical due diligence support for Business Development.</li>
<li>Experience in Investigative Toxicology and preclinical development of ophthalmology, pulmonary or Gene Therapy drugs is highly desirable.</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
|
|
|
|
|
Jul 20th, 2020 03:28PM
|
Jul 20th, 2020 03:28PM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Jul 27th, 2020 12:00AM
|
Toxicology/DMPK, Senior Scientist
|
Open
|
Pharmacology
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jul 21st, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates (designed to be eukaryotic ribosomal selective glycosides or ERSGs) that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons have been identified in over 1,800 rare and ultra-rare diseases.
<p>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. ELX-02 is an investigational drug that has not been approved by any global regulatory body. Eloxx’s preclinical candidate pool consists of a library of novel drug candidates designed to be ERSGs identified based on read-through potential. Eloxx also has preclinical programs focused on rare ocular genetic disorders and polycystic kidney disease.</p>
<p>Eloxx is headquartered in Waltham, MA, with operations in Rehovot, Israel and Morristown, NJ. &nbsp;For more information, please visit <u>www.eloxxpharma.com</u>.</p>
&nbsp;</div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>The Senior Scientist Toxicology is responsible for timely and effective drug safety and/or pharmacokinetic support for preclinical programs. The incumbent is expected to demonstrate competency in interpreting toxicology/ drug metabolism and pharmacokinetics (DMPK)&nbsp;data, development and implementation of strategic plans for pre- and non-clinical development, as well as providing expertise and guidance in Toxicology/DMPK to project and program teams.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text">This individual will be highly analytical, decisive, goal-oriented, and timeline sensitive while maintaining the highest of scientific and ethical standards. Reporting to the Vice President of Research, the Senior Scientist Toxicology will actively participate on project/program/product teams, as well as collaborate with research leadership on reviewing new business initiatives and opportunities.</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><br><strong>Responsibilities:<br></strong></div>
<div class="generic-details-text">
<ul>
<li>Review and approve Toxicology/DMPK study protocols, reports, associated data.</li>
<li>Nonclinical summaries, Regulatory submission sections and associated documentation.</li>
<li>Design, manage, analyze, review, summarize, interpret and report results of Toxicology, Safety Pharmacology and DMPK studies generated through partner CROs.</li>
<li>Maintain up-to-date Toxicology and/or DMPK plans (linked to overall program plans) for all projects/programs/products, including listings of studies, timelines, status and costs; update and refine as necessary.</li>
<li>Provide scientific/technical due diligence support for Business Development activities as required.</li>
<li>Assist in preparation for regulatory agency interactions.</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Qualifications:</strong></div>
<div class="generic-details-text">
<ul>
<li>Demonstrated knowledge of global regulatory requirements and expectations for nonclinical safety assessment packages to support first in human studies, including thorough knowledge of GLP, GCP, ICH and other applicable global guidelines.</li>
<li>Extensive experience in the outsourcing and external oversight of nonclinical Toxicology/DMPK studies conducted by qualified suppliers.</li>
<li>Hands-on experience in Toxicology and/or DMPK study conduct including general, genetic, developmental and reproductive toxicology, carcinogenicity, toxicokinetics, ADME and safety pharmacology.</li>
<li>Experience representing function to global regulatory agencies in support of IND/CTA submissions.</li>
</ul>
</div>
<div class="generic-details-text">&nbsp;</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Ability to define problems, design experiments, analyze and interpret results.</li>
<li>Ability to prioritize responsibilities and meet deadlines.</li>
<li>Ability to self-motivate and work independently.</li>
<li>Strong attention to detail, experience in monitoring work to assure quality, accuracy and thoroughness.</li>
<li>Excellent analytical and problem-solving skills.</li>
<li>Demonstrated ability to work on complex problems and business processes in which the analysis of situations and/or data frequently requires an in-depth evaluation of multiple, interdependent factors and professional judgment.</li>
<li>Excellent communication skills with an ability to communicate across a variety of audiences including team members, cross-functional project teams, leaders, vendors and senior management.</li>
<li>Ability to work at the strategic and tactical level.</li>
<li>Enthusiastic, positive, upbeat “can do” attitude; doesn’t take themselves too seriously, has a sense of humor and is a team player.</li>
<li>The ability to work well in a fast paced, innovative and performance driven environment.</li>
<li></li>
</ul>
<strong>Experience/Education:</strong>
<ul>
<li>PhD in a related subject, with DABT certification preferred, but not required.</li>
<li>3+ years industry-related experience in regulatory Toxicology and DMPK working within Biotech and pharmaceutical industry.</li>
<li>Experience with both small and macromolecular/biologic drugs is highly desirable.</li>
<li>Experience in providing formal scientific/technical due diligence support for Business Development.</li>
<li>Experience in Investigative Toxicology and preclinical development of ophthalmology, pulmonary or Gene Therapy drugs is highly desirable.</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
|
|
|
|
|
Jul 27th, 2020 03:06PM
|
Jul 27th, 2020 03:06PM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Jun 9th, 2020 12:00AM
|
Director, Program Management - Contract
|
Open
|
Program Management
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jun 8th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons are point mutations that disrupt protein synthesis from messenger RNA. As a consequence, patients with premature stop codon diseases have reduced or eliminated protein production from the mutation bearing allele accounting for some of the most severe phenotypes in these genetic diseases. These premature stop codons have been identified in over 1,800 rare and ultra-rare diseases. Read-through therapeutic development is focused on extending mRNA half-life and increasing protein synthesis by enabling the cytoplasmic ribosome to read through premature stop codons to produce full-length proteins.<br><br>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. Eloxx’s preclinical candidate pool consists of a library of novel ERSG drug candidates identified based on read-through potential. Eloxx recently announced a new program focused on rare ocular genetic disorders.<br><br>Eloxx Pharmaceuticals (ELOX) is a Nasdaq listed biotechnology company headquartered in Waltham, MA with regional operations in New Jersey and Tel Aviv Israel.<br><br></div>
<div class="generic-details-text"> </div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>Eloxx Pharmaceuticals is looking for Director of Program Management -Contractor to lead cross-functional projects in a fast-paced environment. The expected contract will be 5 – 6 months with the possibility to extend. This roles will be responsible for maintaining, integrating and executing plans, schedules and budgets for all of Eloxx’s disease areas. This is a highly visible role, working closely with the CEO to make a big impact on the success of our program teams while our Lead Program Manager is on maternity leave. </div>
<div class="generic-details-text"> </div>
<div class="generic-details-text">This position is based in our Waltham, MA Headquarters although remote work is currently an option.</div>
<div class="generic-details-text"><br><br><strong>Responsibilities:<br></strong>
<ul>
<li>Maintain study tracking tools, decision logs and study calendars to ensure deadlines and deliverables are met on or ahead of schedule</li>
<li>Compile budgets and track actual expenditures</li>
<li>Meet with functional heads regularly to capture progress updates on individual tasks and ensure sub-team timelines are aligned with overall project timelines across multiple programs</li>
<li>Coordinate core team meetings, including setting agendas, capturing meeting minutes, and ensuring appropriate follow-up for action items.</li>
<li>Identify and anticipate challenges, assist in developing risk assessment and mitigation plans by working closely with cross-functional team leads and appropriately elevating issues in a timely manner</li>
<li>Serve as lead CMC Project Manager responsible for monitoring and directing work, tracking and approving invoices, and managing material inventory and distribution of materials per program plans</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Excellent communication and interpersonal skills</li>
<li>Aptitude for organizational detail and ability to manage multiple projects</li>
<li>Ability to interact across all levels of the organization</li>
<li>Capacity to complete tasks independently in a highly-regulated environment</li>
<li>Flexibility to function well within a team environment and within condensed timelines</li>
<li>Ability to verbalize complex study issues and demonstrated problem-solving ability</li>
</ul>
<strong><br>Experience/Education:</strong>
<ul>
<li>B.S. in a relevant field with 5+ years of direct Project/Program Management experience in the pharmaceutical or biotechnology industry, CMC experience is preferred but not required</li>
<li>PMP Certification preferred</li>
<li>Experience overseeing and coordinating with consultants/vendors</li>
<li>Experience tracking task completion, working with various functional areas to drive timelines and identify/escalate issues and risks</li>
<li>Experience leading cross-functional team meetings</li>
<li>Experience with related software is a plus but is not required: smartsheets, MS project, MS Timeline, OneNote, SharePoint</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
</div>
|
|
|
|
|
Jun 9th, 2020 01:35PM
|
Jun 9th, 2020 01:35PM
|
Eloxx Pharmaceuticals
|
|
|
|
nasdaq:elox
|
www.eloxxpharma.com
|
www.eloxxpharma.com
|
Jun 10th, 2020 12:00AM
|
Contract Program Manager
|
Open
|
Program Management
|
|
Waltham, Massachusetts, United States
|
Waltham
|
MA
|
USA
|
Jun 8th, 2020 12:00AM
|
|
<div class="generic-details-text"><strong>The Company:<br></strong>Eloxx Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing novel RNA-modulating drug candidates that are formulated to treat rare and ultra-rare premature stop codon diseases. Premature stop codons are point mutations that disrupt protein synthesis from messenger RNA. As a consequence, patients with premature stop codon diseases have reduced or eliminated protein production from the mutation bearing allele accounting for some of the most severe phenotypes in these genetic diseases. These premature stop codons have been identified in over 1,800 rare and ultra-rare diseases. Read-through therapeutic development is focused on extending mRNA half-life and increasing protein synthesis by enabling the cytoplasmic ribosome to read through premature stop codons to produce full-length proteins.<br><br>Eloxx’s lead investigational product candidate, ELX-02, is a small molecule drug candidate designed to restore production of full-length functional proteins. ELX-02 is in the early stages of clinical development, currently focusing on cystic fibrosis. Eloxx’s preclinical candidate pool consists of a library of novel ERSG drug candidates identified based on read-through potential. Eloxx recently announced a new program focused on rare ocular genetic disorders.<br><br>Eloxx Pharmaceuticals (ELOX) is a Nasdaq listed biotechnology company headquartered in Waltham, MA with regional operations in New Jersey and Tel Aviv Israel.<br><br></div>
<div class="generic-details-text"> </div>
<div class="generic-details-text"><strong><strong><br>The Role:<br></strong></strong>Eloxx Pharmaceuticals is looking for a Contract Program Manager to lead cross-functional projects in a fast-paced environment. The Contract Program Manager maintains, integrates and executes plans, schedules and budgets for all of Eloxx’s disease areas. This is a highly visible role, working closely with the CEO to make a big impact on the success of our program teams while our Lead Program Manager is on maternity leave. The expected contract will be 5 – 6 months with the possibility to extend.<strong><strong><br></strong></strong> </div>
<div class="generic-details-text">This position is based in our Waltham, MA Headquarters although remote work is currently an option.</div>
<div class="generic-details-text"><br><br><strong>Responsibilities:<br></strong>
<ul>
<li>Maintain study tracking tools, decision logs and study calendars to ensure deadlines and deliverables are met on or ahead of schedule</li>
<li>Compile budgets and track actual expenditures</li>
<li>Meet with functional heads regularly to capture progress updates on individual tasks and ensure sub-team timelines are aligned with overall project timelines across multiple programs</li>
<li>Coordinate core team meetings, including setting agendas, capturing meeting minutes, and ensuring appropriate follow-up for action items.</li>
<li>Identify and anticipate challenges, assist in developing risk assessment and mitigation plans by working closely with cross-functional team leads and appropriately elevating issues in a timely manner</li>
<li>Serve as lead CMC Project Manager responsible for monitoring and directing work, tracking and approving invoices, and managing material inventory and distribution of materials per program plans</li>
</ul>
<pre> </pre>
</div>
<div class="generic-details-text"><strong>Competencies Include:</strong>
<ul>
<li>Excellent communication and interpersonal skills</li>
<li>Aptitude for organizational detail and ability to manage multiple projects</li>
<li>Ability to interact across all levels of the organization</li>
<li>Capacity to complete tasks independently in a highly-regulated environment</li>
<li>Flexibility to function well within a team environment and within condensed timelines</li>
<li>Ability to verbalize complex study issues and demonstrated problem-solving ability</li>
</ul>
<strong><br>Experience/Education:</strong>
<ul>
<li>B.S. in a relevant field with 5+ years of direct Project/Program Management experience in the pharmaceutical or biotechnology industry, CMC experience is preferred but not required</li>
<li>PMP Certification preferred</li>
<li>Experience overseeing and coordinating with consultants/vendors</li>
<li>Experience tracking task completion, working with various functional areas to drive timelines and identify/escalate issues and risks</li>
<li>Experience leading cross-functional team meetings</li>
<li>Experience with related software is a plus but is not required: smartsheets, MS project, MS Timeline, OneNote, SharePoint</li>
</ul>
<strong><br></strong>
<p><em>Eloxx Pharmaceuticals is an Equal Opportunity Employer and does not discriminate against applicants due to race, ethnicity, gender, veteran status, or on the basis of disability or any other federal, state or local protected class.</em></p>
<p style="text-align: left;"><em>Employment agencies are an important component to our talent acquisition strategy, and we value the partnerships we have built with our preferred vendors. We will not accept unsolicited resumes from employment agencies for any employment opportunity. All resumes submitted by search firms to any employee at Eloxx or directly to hiring managers in any form without a signed Eloxx Employment Agency Agreement on file and search engagement for that position, will be deemed unsolicited in nature, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means.</em></p>
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Jun 10th, 2020 01:22PM
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Jun 10th, 2020 01:22PM
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Eloxx Pharmaceuticals
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