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Adverum Biotechnologies

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# Ticker Symbol Entity Name Domain As Of Date Title URL Brand Category Location Text City State Country Posted Date Number of Openings Description Date Added Date Updated Ticker Sector Ticker Industry
1 nasdaq:advm adverum.com adverum.com Jul 2nd, 2018 12:00AM Senior Manager, Project and Portfolio Management Open Project and Portfolio Management Menlo Park, CA, United States Menlo Park CA USA Jun 11th, 2018 12:00AM <p><strong><u>Senior Manager, Project and Portfolio Management</u></strong></p> <p>Adverum Biotechnologies is a gene therapy company committed to discovering and developing novel medicines that can offer life-changing benefits to patients living with rare diseases or diseases of the eye who currently have limited or burdensome treatment options</p> <p>The Senior Manager, Project and Portfolio Management (PPM) will:</p> <ul> <li>Be responsible for managing one or more highly complex development projects; co-lead early stage development team(s) with a project team leader to drive preclinical assets into the clinic.</li> <li>Work closely with the project team members representing preclinical, clinical, regulatory, and operations, CMC, quality, legal departments in a matrix team environment to develop concise strategic development proposals, integrated project plans, and manage and track key project deliverables.</li> <li>Provide regular project team deliverables and progress updates to Senior Management</li> <li>Report into the Senior Director, Project and Portfolio Management.</li> </ul> <p><strong>Essential duties and responsibilities include but are not limited to the following:</strong></p> <ul> <li>Work with the Project Leader to proactively facilitate team discussions on project strategies, short-term and long-term project planning, opportunities for expediting timelines, identification resource constraints, and proactively identify complex project issues and risks, and assure appropriate escalation.</li> <li>Schedule and facilitate Cross-Functional Project Team meetings using meeting management best practices to drive cross-functional communication, timely and effective decision-making, and successful execution of program objectives. Develop agendas and summarize key meeting discussions and decisions (meeting minutes).</li> <li>Develop, track and maintain project development timelines, deliverables and milestones; including understanding and communicating inter-dependencies and critical path activities.</li> <li>Develop, track and maintain project publication plans, work with team to identify key conferences and journals, coordinate publication development and publication gap analysis.</li> <li>Work closely with and build strong working relationships with cross-functional team members to develop a collaborative team environment and manage timelines for regulatory submissions (IND/NDA/BLA/MAA, etc.).</li> <li>Assists in the review of project team regulatory documents and SOP revisions, if relevant.</li> <li>Work closely with Sr. Director PPM in ongoing enhancements and development of team processes, structures, and project reporting tools.</li> </ul> <p><strong>Position Requirements and Experience:</strong></p> <ul> <li>BS required; Masters Degree Preferred.</li> <li>5+ years of project management experience, with a minimum of 3 years in early and/or late stage drug development project management.</li> <li>Exposure to early-stage programs (pre-clinical though Phase I/II proof-of-concept) essential; and exposure to late-stage programs (Phase II/III pivotal) a plus.</li> <li>Able to work independently with minimal oversight</li> <li>Proven ability to balance the strategic needs of the program with tactical day-to-day activities.</li> <li>Ability to analyze complex activities and information to help guide decision-making that meets the overall objectives and long-range plans of projects and the organization</li> <li>Excellent people (soft) skills, diplomacy and positive influencing abilities.</li> <li>Gene therapy and rare disease experience preferred.</li> <li>Ability to proactively predict issues and solve problems, identify risks.</li> <li>Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix team.</li> <li>Understanding of US and EU Regulatory requirements.</li> <li>Outstanding communication, planning and organizational skills.</li> <li>Highly collaborative team player who fosters open communication and able to facilitate urgent needs.</li> <li>Successful track record of creating and managing accurate timelines and the use of project software (Microsoft Project, Visio, PowerPoint and Excel, etc.).</li> </ul> Jul 1st, 2018 10:12PM Jul 1st, 2018 10:12PM Health Care Equipment & Services
2 nasdaq:advm adverum.com adverum.com Jul 1st, 2018 12:00AM Senior Manager, Project and Portfolio Management Open Project and Portfolio Management Menlo Park, CA, United States Menlo Park CA USA Jun 11th, 2018 12:00AM <p><strong><u>Senior Manager, Project and Portfolio Management</u></strong></p> <p>Adverum Biotechnologies is a gene therapy company committed to discovering and developing novel medicines that can offer life-changing benefits to patients living with rare diseases or diseases of the eye who currently have limited or burdensome treatment options</p> <p>The Senior Manager, Project and Portfolio Management (PPM) will:</p> <ul> <li>Be responsible for managing one or more highly complex development projects; co-lead early stage development team(s) with a project team leader to drive preclinical assets into the clinic.</li> <li>Work closely with the project team members representing preclinical, clinical, regulatory, and operations, CMC, quality, legal departments in a matrix team environment to develop concise strategic development proposals, integrated project plans, and manage and track key project deliverables.</li> <li>Provide regular project team deliverables and progress updates to Senior Management</li> <li>Report into the Senior Director, Project and Portfolio Management.</li> </ul> <p><strong>Essential duties and responsibilities include but are not limited to the following:</strong></p> <ul> <li>Work with the Project Leader to proactively facilitate team discussions on project strategies, short-term and long-term project planning, opportunities for expediting timelines, identification resource constraints, and proactively identify complex project issues and risks, and assure appropriate escalation.</li> <li>Schedule and facilitate Cross-Functional Project Team meetings using meeting management best practices to drive cross-functional communication, timely and effective decision-making, and successful execution of program objectives. Develop agendas and summarize key meeting discussions and decisions (meeting minutes).</li> <li>Develop, track and maintain project development timelines, deliverables and milestones; including understanding and communicating inter-dependencies and critical path activities.</li> <li>Develop, track and maintain project publication plans, work with team to identify key conferences and journals, coordinate publication development and publication gap analysis.</li> <li>Work closely with and build strong working relationships with cross-functional team members to develop a collaborative team environment and manage timelines for regulatory submissions (IND/NDA/BLA/MAA, etc.).</li> <li>Assists in the review of project team regulatory documents and SOP revisions, if relevant.</li> <li>Work closely with Sr. Director PPM in ongoing enhancements and development of team processes, structures, and project reporting tools.</li> </ul> <p><strong>Position Requirements and Experience:</strong></p> <ul> <li>BS required; Masters Degree Preferred.</li> <li>5+ years of project management experience, with a minimum of 3 years in early and/or late stage drug development project management.</li> <li>Exposure to early-stage programs (pre-clinical though Phase I/II proof-of-concept) essential; and exposure to late-stage programs (Phase II/III pivotal) a plus.</li> <li>Able to work independently with minimal oversight</li> <li>Proven ability to balance the strategic needs of the program with tactical day-to-day activities.</li> <li>Ability to analyze complex activities and information to help guide decision-making that meets the overall objectives and long-range plans of projects and the organization</li> <li>Excellent people (soft) skills, diplomacy and positive influencing abilities.</li> <li>Gene therapy and rare disease experience preferred.</li> <li>Ability to proactively predict issues and solve problems, identify risks.</li> <li>Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix team.</li> <li>Understanding of US and EU Regulatory requirements.</li> <li>Outstanding communication, planning and organizational skills.</li> <li>Highly collaborative team player who fosters open communication and able to facilitate urgent needs.</li> <li>Successful track record of creating and managing accurate timelines and the use of project software (Microsoft Project, Visio, PowerPoint and Excel, etc.).</li> </ul> Jun 30th, 2018 10:12PM Jun 30th, 2018 10:12PM Health Care Equipment & Services
3 nasdaq:advm adverum.com adverum.com Jun 30th, 2018 12:00AM Senior Manager, Project and Portfolio Management Open Project and Portfolio Management Menlo Park, CA, United States Menlo Park CA USA Jun 11th, 2018 12:00AM <p><strong><u>Senior Manager, Project and Portfolio Management</u></strong></p> <p>Adverum Biotechnologies is a gene therapy company committed to discovering and developing novel medicines that can offer life-changing benefits to patients living with rare diseases or diseases of the eye who currently have limited or burdensome treatment options</p> <p>The Senior Manager, Project and Portfolio Management (PPM) will:</p> <ul> <li>Be responsible for managing one or more highly complex development projects; co-lead early stage development team(s) with a project team leader to drive preclinical assets into the clinic.</li> <li>Work closely with the project team members representing preclinical, clinical, regulatory, and operations, CMC, quality, legal departments in a matrix team environment to develop concise strategic development proposals, integrated project plans, and manage and track key project deliverables.</li> <li>Provide regular project team deliverables and progress updates to Senior Management</li> <li>Report into the Senior Director, Project and Portfolio Management.</li> </ul> <p><strong>Essential duties and responsibilities include but are not limited to the following:</strong></p> <ul> <li>Work with the Project Leader to proactively facilitate team discussions on project strategies, short-term and long-term project planning, opportunities for expediting timelines, identification resource constraints, and proactively identify complex project issues and risks, and assure appropriate escalation.</li> <li>Schedule and facilitate Cross-Functional Project Team meetings using meeting management best practices to drive cross-functional communication, timely and effective decision-making, and successful execution of program objectives. Develop agendas and summarize key meeting discussions and decisions (meeting minutes).</li> <li>Develop, track and maintain project development timelines, deliverables and milestones; including understanding and communicating inter-dependencies and critical path activities.</li> <li>Develop, track and maintain project publication plans, work with team to identify key conferences and journals, coordinate publication development and publication gap analysis.</li> <li>Work closely with and build strong working relationships with cross-functional team members to develop a collaborative team environment and manage timelines for regulatory submissions (IND/NDA/BLA/MAA, etc.).</li> <li>Assists in the review of project team regulatory documents and SOP revisions, if relevant.</li> <li>Work closely with Sr. Director PPM in ongoing enhancements and development of team processes, structures, and project reporting tools.</li> </ul> <p><strong>Position Requirements and Experience:</strong></p> <ul> <li>BS required; Masters Degree Preferred.</li> <li>5+ years of project management experience, with a minimum of 3 years in early and/or late stage drug development project management.</li> <li>Exposure to early-stage programs (pre-clinical though Phase I/II proof-of-concept) essential; and exposure to late-stage programs (Phase II/III pivotal) a plus.</li> <li>Able to work independently with minimal oversight</li> <li>Proven ability to balance the strategic needs of the program with tactical day-to-day activities.</li> <li>Ability to analyze complex activities and information to help guide decision-making that meets the overall objectives and long-range plans of projects and the organization</li> <li>Excellent people (soft) skills, diplomacy and positive influencing abilities.</li> <li>Gene therapy and rare disease experience preferred.</li> <li>Ability to proactively predict issues and solve problems, identify risks.</li> <li>Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix team.</li> <li>Understanding of US and EU Regulatory requirements.</li> <li>Outstanding communication, planning and organizational skills.</li> <li>Highly collaborative team player who fosters open communication and able to facilitate urgent needs.</li> <li>Successful track record of creating and managing accurate timelines and the use of project software (Microsoft Project, Visio, PowerPoint and Excel, etc.).</li> </ul> Jun 29th, 2018 10:15PM Jun 29th, 2018 10:15PM Health Care Equipment & Services
4 nasdaq:advm adverum.com adverum.com Jun 29th, 2018 12:00AM Senior Manager, Project and Portfolio Management Open Project and Portfolio Management Menlo Park, CA, United States Menlo Park CA USA Jun 11th, 2018 12:00AM <p><strong><u>Senior Manager, Project and Portfolio Management</u></strong></p> <p>Adverum Biotechnologies is a gene therapy company committed to discovering and developing novel medicines that can offer life-changing benefits to patients living with rare diseases or diseases of the eye who currently have limited or burdensome treatment options</p> <p>The Senior Manager, Project and Portfolio Management (PPM) will:</p> <ul> <li>Be responsible for managing one or more highly complex development projects; co-lead early stage development team(s) with a project team leader to drive preclinical assets into the clinic.</li> <li>Work closely with the project team members representing preclinical, clinical, regulatory, and operations, CMC, quality, legal departments in a matrix team environment to develop concise strategic development proposals, integrated project plans, and manage and track key project deliverables.</li> <li>Provide regular project team deliverables and progress updates to Senior Management</li> <li>Report into the Senior Director, Project and Portfolio Management.</li> </ul> <p><strong>Essential duties and responsibilities include but are not limited to the following:</strong></p> <ul> <li>Work with the Project Leader to proactively facilitate team discussions on project strategies, short-term and long-term project planning, opportunities for expediting timelines, identification resource constraints, and proactively identify complex project issues and risks, and assure appropriate escalation.</li> <li>Schedule and facilitate Cross-Functional Project Team meetings using meeting management best practices to drive cross-functional communication, timely and effective decision-making, and successful execution of program objectives. Develop agendas and summarize key meeting discussions and decisions (meeting minutes).</li> <li>Develop, track and maintain project development timelines, deliverables and milestones; including understanding and communicating inter-dependencies and critical path activities.</li> <li>Develop, track and maintain project publication plans, work with team to identify key conferences and journals, coordinate publication development and publication gap analysis.</li> <li>Work closely with and build strong working relationships with cross-functional team members to develop a collaborative team environment and manage timelines for regulatory submissions (IND/NDA/BLA/MAA, etc.).</li> <li>Assists in the review of project team regulatory documents and SOP revisions, if relevant.</li> <li>Work closely with Sr. Director PPM in ongoing enhancements and development of team processes, structures, and project reporting tools.</li> </ul> <p><strong>Position Requirements and Experience:</strong></p> <ul> <li>BS required; Masters Degree Preferred.</li> <li>5+ years of project management experience, with a minimum of 3 years in early and/or late stage drug development project management.</li> <li>Exposure to early-stage programs (pre-clinical though Phase I/II proof-of-concept) essential; and exposure to late-stage programs (Phase II/III pivotal) a plus.</li> <li>Able to work independently with minimal oversight</li> <li>Proven ability to balance the strategic needs of the program with tactical day-to-day activities.</li> <li>Ability to analyze complex activities and information to help guide decision-making that meets the overall objectives and long-range plans of projects and the organization</li> <li>Excellent people (soft) skills, diplomacy and positive influencing abilities.</li> <li>Gene therapy and rare disease experience preferred.</li> <li>Ability to proactively predict issues and solve problems, identify risks.</li> <li>Ability to drive decision-making within a multi-disciplinary, multi-regional, matrix team.</li> <li>Understanding of US and EU Regulatory requirements.</li> <li>Outstanding communication, planning and organizational skills.</li> <li>Highly collaborative team player who fosters open communication and able to facilitate urgent needs.</li> <li>Successful track record of creating and managing accurate timelines and the use of project software (Microsoft Project, Visio, PowerPoint and Excel, etc.).</li> </ul> Jun 28th, 2018 10:15PM Jun 28th, 2018 10:15PM Health Care Equipment & Services
5 nasdaq:advm adverum.com adverum.com Mar 20th, 2019 12:00AM Associate Scientist, Assay Development Open Assay Development Menlo Park, CA, United States Menlo Park CA USA Mar 19th, 2019 12:00AM <p>Adverum is a clinical-stage gene therapy company targeting unmet medical needs in ophthalmology and rare diseases. Adverum develops gene therapy product candidates designed to provide durable efficacy by inducing sustained expression of a therapeutic protein. Adverum has collaboration agreements with Regeneron Pharmaceuticals to research, develop, and commercialize gene therapy products for ophthalmic diseases and Editas Medicine to explore the delivery of genome editing medicines for the treatment of inherited retinal diseases. Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.</p> <p>Our Assay Development team is looking to bring onboard a highly motivated Associate Scientist to support the R&amp;D group in an industry setting. The candidate would particularly be involved in quantitative assay development and performance in a variety of formats in support of pharmacokinetics, pharmacodynamics, and product release.</p> <p><strong>Core Job Responsibilities:</strong></p> <ul> <li>Primarily develop, optimize and help qualify qPCR and other molecular biology assays, as well as support the development of cell-based assays.</li> <li>Work collaboratively with different research and development departments to evaluate and implement new assay formats and/or technologies.</li> <li>Perform some testing as needed in support of product characterization and preclinical studies.</li> <li>Transfer of assays to and oversight of work at Contract Research Organizations will be required.</li> <li>Responsibilities will also include routine lab maintenance, writing test procedures, SOPs, protocols, technical reports, and summarizing/presenting data at internal and external meetings.</li> <li>Maintaining good documentation is required.</li> </ul> <p><strong>Core Requirements:</strong></p> <ul> <li>Minimum of a biological science bachelor’s degree with 4-5 years’ experience in a biotech company, or a master’s degree with 2-3 years’ experience, or an equivalent combination of education and experience.</li> <li>Experience in assay development is required</li> <li>Expertise in a variety of laboratory techniques involving recombinant DNA technology (cloning, transformation, qPCR, primer and probe design, DNA/RNA isolation and analysis; qPCR data analysis) sterile tissue culture techniques (transfection, transduction, maintaining cell lines) is required</li> <li>Experience in biochemical techniques such as Western Blot, ELISA, flow cytometry, and immunofluorescence is strongly desired</li> <li>Broad knowledge of molecular biology and/or protein assay methods and biochemistry with application to gene therapy is strongly desired</li> <li>Experience in the qualification/validation of quantitative assays is desired</li> <li>Background in the area of retinal or genetic diseases is desired, with an understanding of AAV biology a plus</li> <li>Publication in a peer-reviewed journal or having presented at a conference is desired</li> <li>Experience in tissue handling is preferred</li> <li>Must be a self-starter, proactive, co-operative, and proficient at working both independently and in a small team environment</li> <li>Proven initiative and demonstrated accountability in a fast-paced environment with high degree of flexibility.</li> <li>Detail oriented and with time management skills</li> <li>Excellent verbal and written communication skills</li> <li>Proficiency with SoftMaxPro, GraphPad Prism, and other common analytical software desired</li> <li>Proficient with MS Office and other common office software</li> </ul> Mar 19th, 2019 10:06PM Mar 19th, 2019 10:06PM Health Care Equipment & Services
6 nasdaq:advm adverum.com adverum.com Mar 19th, 2019 12:00AM Associate Scientist, Assay Development Open Assay Development Menlo Park, CA, United States Menlo Park CA USA Feb 13th, 2019 12:00AM <p>Adverum is a clinical-stage gene therapy company targeting unmet medical needs in ophthalmology and rare diseases. Adverum develops gene therapy product candidates designed to provide durable efficacy by inducing sustained expression of a therapeutic protein. Adverum has collaboration agreements with Regeneron Pharmaceuticals to research, develop, and commercialize gene therapy products for ophthalmic diseases and Editas Medicine to explore the delivery of genome editing medicines for the treatment of inherited retinal diseases. Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.</p> <p>Our Assay Development team is looking to bring onboard a highly motivated Associate Scientist to support the R&amp;D group in an industry setting. The candidate would particularly be involved in quantitative assay development and performance in a variety of formats in support of pharmacokinetics, pharmacodynamics, and product release.</p> <p><strong>Core Job Responsibilities:</strong></p> <ul> <li>Primarily develop, optimize and help qualify qPCR and other molecular biology assays, as well as support the development of cell-based assays.</li> <li>Work collaboratively with different research and development departments to evaluate and implement new assay formats and/or technologies.</li> <li>Perform some testing as needed in support of product characterization and preclinical studies.</li> <li>Transfer of assays to and oversight of work at Contract Research Organizations will be required.</li> <li>Responsibilities will also include routine lab maintenance, writing test procedures, SOPs, protocols, technical reports, and summarizing/presenting data at internal and external meetings.</li> <li>Maintaining good documentation is required.</li> </ul> <p><strong>Core Requirements:</strong></p> <ul> <li>Minimum of a biological science bachelor’s degree with 4-5 years’ experience in a biotech company, or a master’s degree with 2-3 years’ experience, or an equivalent combination of education and experience.</li> <li>Experience in assay development is required</li> <li>Expertise in a variety of laboratory techniques involving recombinant DNA technology (cloning, transformation, qPCR, primer and probe design, DNA/RNA isolation and analysis; qPCR data analysis) sterile tissue culture techniques (transfection, transduction, maintaining cell lines) is required</li> <li>Experience in biochemical techniques such as Western Blot, ELISA, flow cytometry, and immunofluorescence is strongly desired</li> <li>Broad knowledge of molecular biology and/or protein assay methods and biochemistry with application to gene therapy is strongly desired</li> <li>Experience in the qualification/validation of quantitative assays is desired</li> <li>Background in the area of retinal or genetic diseases is desired, with an understanding of AAV biology a plus</li> <li>Publication in a peer-reviewed journal or having presented at a conference is desired</li> <li>Experience in tissue handling is preferred</li> <li>Must be a self-starter, proactive, co-operative, and proficient at working both independently and in a small team environment</li> <li>Proven initiative and demonstrated accountability in a fast-paced environment with high degree of flexibility.</li> <li>Detail oriented and with time management skills</li> <li>Excellent verbal and written communication skills</li> <li>Proficiency with SoftMaxPro, GraphPad Prism, and other common analytical software desired</li> <li>Proficient with MS Office and other common office software</li> </ul> Mar 18th, 2019 10:06PM Mar 18th, 2019 10:06PM Health Care Equipment & Services
7 nasdaq:advm adverum.com adverum.com Mar 18th, 2019 12:00AM Associate Scientist, Assay Development Open Assay Development Menlo Park, CA, United States Menlo Park CA USA Feb 13th, 2019 12:00AM <p>Adverum is a clinical-stage gene therapy company targeting unmet medical needs in ophthalmology and rare diseases. Adverum develops gene therapy product candidates designed to provide durable efficacy by inducing sustained expression of a therapeutic protein. Adverum has collaboration agreements with Regeneron Pharmaceuticals to research, develop, and commercialize gene therapy products for ophthalmic diseases and Editas Medicine to explore the delivery of genome editing medicines for the treatment of inherited retinal diseases. Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.</p> <p>Our Assay Development team is looking to bring onboard a highly motivated Associate Scientist to support the R&amp;D group in an industry setting. The candidate would particularly be involved in quantitative assay development and performance in a variety of formats in support of pharmacokinetics, pharmacodynamics, and product release.</p> <p><strong>Core Job Responsibilities:</strong></p> <ul> <li>Primarily develop, optimize and help qualify qPCR and other molecular biology assays, as well as support the development of cell-based assays.</li> <li>Work collaboratively with different research and development departments to evaluate and implement new assay formats and/or technologies.</li> <li>Perform some testing as needed in support of product characterization and preclinical studies.</li> <li>Transfer of assays to and oversight of work at Contract Research Organizations will be required.</li> <li>Responsibilities will also include routine lab maintenance, writing test procedures, SOPs, protocols, technical reports, and summarizing/presenting data at internal and external meetings.</li> <li>Maintaining good documentation is required.</li> </ul> <p><strong>Core Requirements:</strong></p> <ul> <li>Minimum of a biological science bachelor’s degree with 4-5 years’ experience in a biotech company, or a master’s degree with 2-3 years’ experience, or an equivalent combination of education and experience.</li> <li>Experience in assay development is required</li> <li>Expertise in a variety of laboratory techniques involving recombinant DNA technology (cloning, transformation, qPCR, primer and probe design, DNA/RNA isolation and analysis; qPCR data analysis) sterile tissue culture techniques (transfection, transduction, maintaining cell lines) is required</li> <li>Experience in biochemical techniques such as Western Blot, ELISA, flow cytometry, and immunofluorescence is strongly desired</li> <li>Broad knowledge of molecular biology and/or protein assay methods and biochemistry with application to gene therapy is strongly desired</li> <li>Experience in the qualification/validation of quantitative assays is desired</li> <li>Background in the area of retinal or genetic diseases is desired, with an understanding of AAV biology a plus</li> <li>Publication in a peer-reviewed journal or having presented at a conference is desired</li> <li>Experience in tissue handling is preferred</li> <li>Must be a self-starter, proactive, co-operative, and proficient at working both independently and in a small team environment</li> <li>Proven initiative and demonstrated accountability in a fast-paced environment with high degree of flexibility.</li> <li>Detail oriented and with time management skills</li> <li>Excellent verbal and written communication skills</li> <li>Proficiency with SoftMaxPro, GraphPad Prism, and other common analytical software desired</li> <li>Proficient with MS Office and other common office software</li> </ul> Mar 17th, 2019 10:06PM Mar 17th, 2019 10:06PM Health Care Equipment & Services
8 nasdaq:advm adverum.com adverum.com Mar 17th, 2019 12:00AM Associate Scientist, Assay Development Open Assay Development Menlo Park, CA, United States Menlo Park CA USA Feb 13th, 2019 12:00AM <p>Adverum is a clinical-stage gene therapy company targeting unmet medical needs in ophthalmology and rare diseases. Adverum develops gene therapy product candidates designed to provide durable efficacy by inducing sustained expression of a therapeutic protein. Adverum has collaboration agreements with Regeneron Pharmaceuticals to research, develop, and commercialize gene therapy products for ophthalmic diseases and Editas Medicine to explore the delivery of genome editing medicines for the treatment of inherited retinal diseases. Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.</p> <p>Our Assay Development team is looking to bring onboard a highly motivated Associate Scientist to support the R&amp;D group in an industry setting. The candidate would particularly be involved in quantitative assay development and performance in a variety of formats in support of pharmacokinetics, pharmacodynamics, and product release.</p> <p><strong>Core Job Responsibilities:</strong></p> <ul> <li>Primarily develop, optimize and help qualify qPCR and other molecular biology assays, as well as support the development of cell-based assays.</li> <li>Work collaboratively with different research and development departments to evaluate and implement new assay formats and/or technologies.</li> <li>Perform some testing as needed in support of product characterization and preclinical studies.</li> <li>Transfer of assays to and oversight of work at Contract Research Organizations will be required.</li> <li>Responsibilities will also include routine lab maintenance, writing test procedures, SOPs, protocols, technical reports, and summarizing/presenting data at internal and external meetings.</li> <li>Maintaining good documentation is required.</li> </ul> <p><strong>Core Requirements:</strong></p> <ul> <li>Minimum of a biological science bachelor’s degree with 4-5 years’ experience in a biotech company, or a master’s degree with 2-3 years’ experience, or an equivalent combination of education and experience.</li> <li>Experience in assay development is required</li> <li>Expertise in a variety of laboratory techniques involving recombinant DNA technology (cloning, transformation, qPCR, primer and probe design, DNA/RNA isolation and analysis; qPCR data analysis) sterile tissue culture techniques (transfection, transduction, maintaining cell lines) is required</li> <li>Experience in biochemical techniques such as Western Blot, ELISA, flow cytometry, and immunofluorescence is strongly desired</li> <li>Broad knowledge of molecular biology and/or protein assay methods and biochemistry with application to gene therapy is strongly desired</li> <li>Experience in the qualification/validation of quantitative assays is desired</li> <li>Background in the area of retinal or genetic diseases is desired, with an understanding of AAV biology a plus</li> <li>Publication in a peer-reviewed journal or having presented at a conference is desired</li> <li>Experience in tissue handling is preferred</li> <li>Must be a self-starter, proactive, co-operative, and proficient at working both independently and in a small team environment</li> <li>Proven initiative and demonstrated accountability in a fast-paced environment with high degree of flexibility.</li> <li>Detail oriented and with time management skills</li> <li>Excellent verbal and written communication skills</li> <li>Proficiency with SoftMaxPro, GraphPad Prism, and other common analytical software desired</li> <li>Proficient with MS Office and other common office software</li> </ul> Mar 16th, 2019 10:05PM Mar 16th, 2019 10:05PM Health Care Equipment & Services
9 nasdaq:advm adverum.com adverum.com Mar 16th, 2019 12:00AM Associate Scientist, Assay Development Open Assay Development Menlo Park, CA, United States Menlo Park CA USA Feb 13th, 2019 12:00AM <p>Adverum is a clinical-stage gene therapy company targeting unmet medical needs in ophthalmology and rare diseases. Adverum develops gene therapy product candidates designed to provide durable efficacy by inducing sustained expression of a therapeutic protein. Adverum has collaboration agreements with Regeneron Pharmaceuticals to research, develop, and commercialize gene therapy products for ophthalmic diseases and Editas Medicine to explore the delivery of genome editing medicines for the treatment of inherited retinal diseases. Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.</p> <p>Our Assay Development team is looking to bring onboard a highly motivated Associate Scientist to support the R&amp;D group in an industry setting. The candidate would particularly be involved in quantitative assay development and performance in a variety of formats in support of pharmacokinetics, pharmacodynamics, and product release.</p> <p><strong>Core Job Responsibilities:</strong></p> <ul> <li>Primarily develop, optimize and help qualify qPCR and other molecular biology assays, as well as support the development of cell-based assays.</li> <li>Work collaboratively with different research and development departments to evaluate and implement new assay formats and/or technologies.</li> <li>Perform some testing as needed in support of product characterization and preclinical studies.</li> <li>Transfer of assays to and oversight of work at Contract Research Organizations will be required.</li> <li>Responsibilities will also include routine lab maintenance, writing test procedures, SOPs, protocols, technical reports, and summarizing/presenting data at internal and external meetings.</li> <li>Maintaining good documentation is required.</li> </ul> <p><strong>Core Requirements:</strong></p> <ul> <li>Minimum of a biological science bachelor’s degree with 4-5 years’ experience in a biotech company, or a master’s degree with 2-3 years’ experience, or an equivalent combination of education and experience.</li> <li>Experience in assay development is required</li> <li>Expertise in a variety of laboratory techniques involving recombinant DNA technology (cloning, transformation, qPCR, primer and probe design, DNA/RNA isolation and analysis; qPCR data analysis) sterile tissue culture techniques (transfection, transduction, maintaining cell lines) is required</li> <li>Experience in biochemical techniques such as Western Blot, ELISA, flow cytometry, and immunofluorescence is strongly desired</li> <li>Broad knowledge of molecular biology and/or protein assay methods and biochemistry with application to gene therapy is strongly desired</li> <li>Experience in the qualification/validation of quantitative assays is desired</li> <li>Background in the area of retinal or genetic diseases is desired, with an understanding of AAV biology a plus</li> <li>Publication in a peer-reviewed journal or having presented at a conference is desired</li> <li>Experience in tissue handling is preferred</li> <li>Must be a self-starter, proactive, co-operative, and proficient at working both independently and in a small team environment</li> <li>Proven initiative and demonstrated accountability in a fast-paced environment with high degree of flexibility.</li> <li>Detail oriented and with time management skills</li> <li>Excellent verbal and written communication skills</li> <li>Proficiency with SoftMaxPro, GraphPad Prism, and other common analytical software desired</li> <li>Proficient with MS Office and other common office software</li> </ul> Mar 15th, 2019 10:06PM Mar 15th, 2019 10:06PM Health Care Equipment & Services
10 nasdaq:advm adverum.com adverum.com Mar 15th, 2019 12:00AM Associate Scientist, Assay Development Open Assay Development Menlo Park, CA, United States Menlo Park CA USA Feb 13th, 2019 12:00AM <p>Adverum is a clinical-stage gene therapy company targeting unmet medical needs in ophthalmology and rare diseases. Adverum develops gene therapy product candidates designed to provide durable efficacy by inducing sustained expression of a therapeutic protein. Adverum has collaboration agreements with Regeneron Pharmaceuticals to research, develop, and commercialize gene therapy products for ophthalmic diseases and Editas Medicine to explore the delivery of genome editing medicines for the treatment of inherited retinal diseases. Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control.</p> <p>Our Assay Development team is looking to bring onboard a highly motivated Associate Scientist to support the R&amp;D group in an industry setting. The candidate would particularly be involved in quantitative assay development and performance in a variety of formats in support of pharmacokinetics, pharmacodynamics, and product release.</p> <p><strong>Core Job Responsibilities:</strong></p> <ul> <li>Primarily develop, optimize and help qualify qPCR and other molecular biology assays, as well as support the development of cell-based assays.</li> <li>Work collaboratively with different research and development departments to evaluate and implement new assay formats and/or technologies.</li> <li>Perform some testing as needed in support of product characterization and preclinical studies.</li> <li>Transfer of assays to and oversight of work at Contract Research Organizations will be required.</li> <li>Responsibilities will also include routine lab maintenance, writing test procedures, SOPs, protocols, technical reports, and summarizing/presenting data at internal and external meetings.</li> <li>Maintaining good documentation is required.</li> </ul> <p><strong>Core Requirements:</strong></p> <ul> <li>Minimum of a biological science bachelor’s degree with 4-5 years’ experience in a biotech company, or a master’s degree with 2-3 years’ experience, or an equivalent combination of education and experience.</li> <li>Experience in assay development is required</li> <li>Expertise in a variety of laboratory techniques involving recombinant DNA technology (cloning, transformation, qPCR, primer and probe design, DNA/RNA isolation and analysis; qPCR data analysis) sterile tissue culture techniques (transfection, transduction, maintaining cell lines) is required</li> <li>Experience in biochemical techniques such as Western Blot, ELISA, flow cytometry, and immunofluorescence is strongly desired</li> <li>Broad knowledge of molecular biology and/or protein assay methods and biochemistry with application to gene therapy is strongly desired</li> <li>Experience in the qualification/validation of quantitative assays is desired</li> <li>Background in the area of retinal or genetic diseases is desired, with an understanding of AAV biology a plus</li> <li>Publication in a peer-reviewed journal or having presented at a conference is desired</li> <li>Experience in tissue handling is preferred</li> <li>Must be a self-starter, proactive, co-operative, and proficient at working both independently and in a small team environment</li> <li>Proven initiative and demonstrated accountability in a fast-paced environment with high degree of flexibility.</li> <li>Detail oriented and with time management skills</li> <li>Excellent verbal and written communication skills</li> <li>Proficiency with SoftMaxPro, GraphPad Prism, and other common analytical software desired</li> <li>Proficient with MS Office and other common office software</li> </ul> Mar 14th, 2019 10:06PM Mar 14th, 2019 10:06PM Health Care Equipment & Services

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