AR

Array BioPharma

- NASDAQ:ARRY
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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:arry www.arraybiopharma.com www.arraybiopharma.com Apr 16th, 2019 12:00AM Director External Manufacturing Quality (Development) Open Development Boulder, CO, US Boulder CO USA Mar 1st, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases. Array markets in the United States BRAFTOVI® (encorafenib) capsules in combination with MEKTOVI® (binimetinib) tablets for the treatment of patients with unresectable or metastatic melanoma with a BRAFV600E or BRAFV600K mutation. Array’s lead clinical programs, encorafenib and binimetinib, are being investigated in over 30 clinical trials across a number of solid tumor indications, including a Phase 3 trial in BRAF-mutant colorectal cancer.

Summary:

Residing in our Boulder, CO office, will provide quality oversight of external contract manufacturers, packagers, and laboratories engaged in early through late phase development of pharmaceutical drug substances and drug products. Will ensure that assigned products are manufactured, packaged, analyzed, released, stored and distributed in accordance with Array standards and all applicable regulatory requirements. This includes change control, deviations/investigations, technical transfers, and product quality oversight of Phase 1, 2, and 3 clinical supplies. Will provide support to ensure effective quality systems at the partner and supports continuous improvement activities.

Responsibilities:

  • The candidate builds and maintains strong relationships with contractors, remains informed of current GMP requirements and industry trends, supports review of regulatory filings, and advises internal departments and contractors on aspects of GMP compliance
  • Acts as the Array Quality point of contact for all quality activities. Implements, maintains and ensures contractor adherence to Array standards and regulatory requirements documented in the Quality Agreement
  • Partners with contractors during regular site visits to address continuous improvement initiatives, remediation efforts, and ongoing projects
  • Function as "Person in Plant" at contractor’s facility to support remediation or routine production
  • Guides contractor investigations of abnormal operational occurrences such as batch rejections, atypical events, quality defects, etc. with support from Supply Chain and Manufacturing, and Regulatory, as required
  • Ensure appropriate handling and filing of contractor records at Array according to document management procedures
  • Reviews and approves contractor documentation including Stability Protocols/Reports, Major and Critical Deviations, Change Controls, Out of specification investigations, Method transfer and validation protocols and reports, process development/transfer protocols and reports, product specifications, master batch records, etc.
  • Supports audits of assigned contractors by assisting in the preparation, observing, and following up on any resulting corrective actions
  • Provides guidance to contractors regarding product compliance, procedures, regulatory requirements and guidelines
  • Reviews relevant drug application modules for accuracy and completeness, verifying source documentation, prior to submission to relevant authorities
  • Ensure execution of the relevant escalation processes and prompt communication of GMP Compliance risks to Array Management

 

Apr 15th, 2019 11:06PM Apr 15th, 2019 11:06PM Health Care Pharmaceuticals & Biotechnology
2 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 17th, 2019 12:00AM Investor Relations & Corporate Communications, Senior Manager Open Gen & Admin Boulder, CO, US Boulder CO USA Feb 7th, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases. Array markets in the United States BRAFTOVI® (encorafenib) capsules in combination with MEKTOVI® (binimetinib) tablets for the treatment of patients with unresectable or metastatic melanoma with a BRAFV600E or BRAFV600K mutation. Array’s lead clinical programs, encorafenib and binimetinib, are being investigated in over 30 clinical trials across a number of solid tumor indications, including a Phase 3 trial in BRAF-mutant colorectal cancer.

Array’s pipeline includes several additional programs being advanced by Array or current license-holders, including the following programs currently in registration trials: selumetinib (partnered with AstraZeneca), LOXO-292 (partnered with Loxo Oncology), ipatasertib (partnered with Genentech), tucatinib (partnered with Seattle Genetics) and ARRY-797. Vitrakvi® (larotrectinib, partnered with Loxo Oncology) is approved in the United States and Ganovo® (danoprevir, partnered with Roche) is approved in China. For more information, please visit www.arraybiopharma.com or follow @arraybiopharma on Twitter and LinkedIn.

Summary:

Residing in our Boulder, CO office, and reporting to the Sr. Director Investor Relations and Corp. Communications, this role will support corporate communications and investor relations in conjunction with external agencies. 

Responsibilities:

Investor Relations:

  • Support investor relations plan and all activities
  • Create and maintain an annual calendar for all conferences, non-road deal shows, updates, etc.
  • Support preparation of all company Press Releases liaising with legal, business and senior management
    • Support quarterly financial results activities, including press releases, slide presentations, conference calls and webcasts
    • Support and filter inbound investor queries and requests
    • Monitor and summarize all company and peer group coverage
    • Supports the development of investor Q&A documents
    • Manages updates to investor pitch book in line with current information

Media Relations:

  • Supports generating coverage in print and broadcast media
  • Prepares executives for media interviews and press conferences
  • Supports press release development and Q&A documents
  • Interface with PR firm to support their activity and deliverables
  • Develops corporate b-roll to support media outreach
  • Monitors the media for relevant corporate, peer and competitive news

Corporate Communications Activities:

  • Coordinates with Array departments to manage and execute internal communications calendar
  • Supports strategy and execution of company meetings
  • Drafts internal communications including email, executive statements and Q&A documents
  • Manages the company’s external website, including strategy, design and content from initial drafting through MLR approval and posting
  • Continually updates the website’s content and graphics in concert with current information
  • Liaises with other Array departments to source content for website as needed

Departmental Support:

  • Coordinates communications with partners to support announcement strategy and tactics
  • Interacts with vendors, agencies, newswire services, Nasdaq and other external partners as needed
  • Supports development of departmental budget
Apr 16th, 2019 11:07PM Apr 16th, 2019 11:07PM Health Care Pharmaceuticals & Biotechnology
3 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 16th, 2019 12:00AM Investor Relations & Corporate Communications, Senior Manager Open Gen & Admin Boulder, CO, US Boulder CO USA Feb 7th, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases. Array markets in the United States BRAFTOVI® (encorafenib) capsules in combination with MEKTOVI® (binimetinib) tablets for the treatment of patients with unresectable or metastatic melanoma with a BRAFV600E or BRAFV600K mutation. Array’s lead clinical programs, encorafenib and binimetinib, are being investigated in over 30 clinical trials across a number of solid tumor indications, including a Phase 3 trial in BRAF-mutant colorectal cancer.

Array’s pipeline includes several additional programs being advanced by Array or current license-holders, including the following programs currently in registration trials: selumetinib (partnered with AstraZeneca), LOXO-292 (partnered with Loxo Oncology), ipatasertib (partnered with Genentech), tucatinib (partnered with Seattle Genetics) and ARRY-797. Vitrakvi® (larotrectinib, partnered with Loxo Oncology) is approved in the United States and Ganovo® (danoprevir, partnered with Roche) is approved in China. For more information, please visit www.arraybiopharma.com or follow @arraybiopharma on Twitter and LinkedIn.

Summary:

Residing in our Boulder, CO office, and reporting to the Sr. Director Investor Relations and Corp. Communications, this role will support corporate communications and investor relations in conjunction with external agencies. 

Responsibilities:

Investor Relations:

  • Support investor relations plan and all activities
  • Create and maintain an annual calendar for all conferences, non-road deal shows, updates, etc.
  • Support preparation of all company Press Releases liaising with legal, business and senior management
    • Support quarterly financial results activities, including press releases, slide presentations, conference calls and webcasts
    • Support and filter inbound investor queries and requests
    • Monitor and summarize all company and peer group coverage
    • Supports the development of investor Q&A documents
    • Manages updates to investor pitch book in line with current information

Media Relations:

  • Supports generating coverage in print and broadcast media
  • Prepares executives for media interviews and press conferences
  • Supports press release development and Q&A documents
  • Interface with PR firm to support their activity and deliverables
  • Develops corporate b-roll to support media outreach
  • Monitors the media for relevant corporate, peer and competitive news

Corporate Communications Activities:

  • Coordinates with Array departments to manage and execute internal communications calendar
  • Supports strategy and execution of company meetings
  • Drafts internal communications including email, executive statements and Q&A documents
  • Manages the company’s external website, including strategy, design and content from initial drafting through MLR approval and posting
  • Continually updates the website’s content and graphics in concert with current information
  • Liaises with other Array departments to source content for website as needed

Departmental Support:

  • Coordinates communications with partners to support announcement strategy and tactics
  • Interacts with vendors, agencies, newswire services, Nasdaq and other external partners as needed
  • Supports development of departmental budget
Apr 15th, 2019 11:06PM Apr 15th, 2019 11:06PM Health Care Pharmaceuticals & Biotechnology
4 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 17th, 2019 12:00AM Research Associate / Associate Scientist - Medicinal Chemistry Open Discovery Boulder, CO, US Boulder CO USA Apr 9th, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company headquartered in Boulder, Colorado. Array is focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases. Array markets in the United States BRAFTOVI®(encorafenib) in combination with MEKTOVI® (binimetinib) for the treatment of patients with unresectable or metastatic melanoma with a BRAFV600E or BRAFV600Kmutation.

Summary:

Array’s medicinal chemistry group has openings for motivated synthetic organic chemists who are able to work in a team environment to deliver quality drug candidates with a sense of urgency.  The ideal candidate will have ability to work closely with others in a collaborative manner.   This role is based in Boulder, CO and is eligible for a relocation package.

Responsibilities:

  • Demonstrates technical competency in reaction set-up, product isolation, purification and analysis, from milligram to multigram scale
  • Work efficiently with minimal supervision in the lab
  • Adhere to all safety requirements
  • Develop an understanding of SAR, contribute to analog design
  • Collaborate closely with colleagues to discuss data and generate new ideas
  • Demonstrate curiosity and interest in furthering knowledge of drug discovery
  • Monitor medicinal and organic chemistry literature
  • Communicate results in written and oral form
  • Practice good lab citizenship
Apr 16th, 2019 11:07PM Apr 16th, 2019 11:07PM Health Care Pharmaceuticals & Biotechnology
5 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 16th, 2019 12:00AM Research Associate / Associate Scientist - Medicinal Chemistry Open Discovery Boulder, CO, US Boulder CO USA Apr 9th, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company headquartered in Boulder, Colorado. Array is focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases. Array markets in the United States BRAFTOVI®(encorafenib) in combination with MEKTOVI® (binimetinib) for the treatment of patients with unresectable or metastatic melanoma with a BRAFV600E or BRAFV600Kmutation.

Summary:

Array’s medicinal chemistry group has openings for motivated synthetic organic chemists who are able to work in a team environment to deliver quality drug candidates with a sense of urgency.  The ideal candidate will have ability to work closely with others in a collaborative manner.   This role is based in Boulder, CO and is eligible for a relocation package.

Responsibilities:

  • Demonstrates technical competency in reaction set-up, product isolation, purification and analysis, from milligram to multigram scale
  • Work efficiently with minimal supervision in the lab
  • Adhere to all safety requirements
  • Develop an understanding of SAR, contribute to analog design
  • Collaborate closely with colleagues to discuss data and generate new ideas
  • Demonstrate curiosity and interest in furthering knowledge of drug discovery
  • Monitor medicinal and organic chemistry literature
  • Communicate results in written and oral form
  • Practice good lab citizenship
Apr 15th, 2019 11:06PM Apr 15th, 2019 11:06PM Health Care Pharmaceuticals & Biotechnology
6 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 17th, 2019 12:00AM Analytical Development and Quality Control Scientist Open Gen & Admin Boulder, CO, US Boulder CO USA Mar 1st, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company headquartered in Boulder, Colorado. Array is focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases.

Summary: 

Residing in our Boulder, CO office, this position provides technical support and oversight of Analytical method development, method validations and stability programs to satisfy the quality and regulatory requirements for small molecule manufacturing and testing in a rapid growth environment.

Responsibilities:

  • Support multiple Array sponsored external contract analytical testing laboratories including the following activities:
    • Oversight of analytical method transfer, development, qualification and validation for small molecule pharmaceutical products. Understands the phase appropriateness of methods and ensures compliance to these standards by the contract labs.
    • Support stability program management including review and approval of protocols, data and author stability reports. Review trends and support setting appropriate expiry dating.
    • Provide input on method troubleshooting and laboratory investigations. Assists in GMP investigations, including deviation root cause analyses, CAPA, and out-of-specification.
    • Exercises sound scientific judgment in selecting methods, techniques, and evaluation criteria for obtaining results for use at contract laboratories.
    • Support the management, transfer and qualification of lab standards and impurities at contract labs.
  • Follows Standard Operating Procedures (SOPs), protocols and other instructions from management.
  • Draft or review organizational appropriate SOPs.
  • Takes ownership of Array analytical methods and specifications including authoring these documents in Array format.
  • Effectively uses the Array document management system including the change control module.
  • Support strategic analytical initiatives in the Supply Chain and Manufacturing organization.
  • Supports process development, specification setting, and CMC regulatory filings and responses as applicable.
  • Support release and stability testing of drug substances and drug products as required.
Apr 16th, 2019 11:07PM Apr 16th, 2019 11:07PM Health Care Pharmaceuticals & Biotechnology
7 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 16th, 2019 12:00AM Analytical Development and Quality Control Scientist Open Gen & Admin Boulder, CO, US Boulder CO USA Mar 1st, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company headquartered in Boulder, Colorado. Array is focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases.

Summary: 

Residing in our Boulder, CO office, this position provides technical support and oversight of Analytical method development, method validations and stability programs to satisfy the quality and regulatory requirements for small molecule manufacturing and testing in a rapid growth environment.

Responsibilities:

  • Support multiple Array sponsored external contract analytical testing laboratories including the following activities:
    • Oversight of analytical method transfer, development, qualification and validation for small molecule pharmaceutical products. Understands the phase appropriateness of methods and ensures compliance to these standards by the contract labs.
    • Support stability program management including review and approval of protocols, data and author stability reports. Review trends and support setting appropriate expiry dating.
    • Provide input on method troubleshooting and laboratory investigations. Assists in GMP investigations, including deviation root cause analyses, CAPA, and out-of-specification.
    • Exercises sound scientific judgment in selecting methods, techniques, and evaluation criteria for obtaining results for use at contract laboratories.
    • Support the management, transfer and qualification of lab standards and impurities at contract labs.
  • Follows Standard Operating Procedures (SOPs), protocols and other instructions from management.
  • Draft or review organizational appropriate SOPs.
  • Takes ownership of Array analytical methods and specifications including authoring these documents in Array format.
  • Effectively uses the Array document management system including the change control module.
  • Support strategic analytical initiatives in the Supply Chain and Manufacturing organization.
  • Supports process development, specification setting, and CMC regulatory filings and responses as applicable.
  • Support release and stability testing of drug substances and drug products as required.
Apr 15th, 2019 11:06PM Apr 15th, 2019 11:06PM Health Care Pharmaceuticals & Biotechnology
8 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 17th, 2019 12:00AM Sr. Manager / Associate Director, Formulation Development Open Gen & Admin Boulder, CO, US Boulder CO USA Mar 1st, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company headquartered in Boulder, Colorado. Array is focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases.

Summary:  Residing in our Boulder, CO office, this position provides technical support and oversight of formulation development, and drug product manufacturing.

Responsibilities:

Support Array sponsored external contract formulation and manufacturing partners including the following activities:

  • Leading formulation tasks or projects to meet the needs for new liquid or solid dosage form development
  • Actively participates in all the phases of development including the pre-formulation, process development, scale-up and support for the transfer to the pilot plant
  • Manage CMO’s for routine GMP production of drug products, including manufacturing, packaging, labeling, and distribution of clinical trial materials
  • Identify, evaluate, and qualify new CMO’s for GMP production of drug products
  • Contribute to studies and/or activities necessary for process optimization and continuous improvement to assure robust and cost-effective manufacturing processes
  • Assure consistent and reproducible manufacturing processes and final drug products
  • Support OOS, root cause, and CAPA investigations, as necessary
  • Manage and execute troubleshooting activities, as necessary
  • Transfer manufacturing operations to alternate sites, as appropriate, to assure continuity of supply
  • Write, review, and approve GMP batch records and protocols
  • Write RFPs, negotiate quotations, and verify invoices are consistent with work performed by CMO’s Work with Legal department to establish agreements and contracts with CMOs
  • Understand and practice good documentation practices in a GMP environment
  • Contribute to preparation and review of regulatory documents for submission to FDA and other regulatory authorities Identify and utilize expert consultants, when necessary
  • Follows Standard Operating Procedures (SOPs), protocols and other instructions from management
  • Execute and review experiment protocols, data summaries, reports
  • Draft or review SOPs, technical documents, analytical method validation protocols and reports
  • Takes a leading role in setting strategic department initiatives
  • Exercises judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results
  • Effectively uses the Array document management system including the change control module
  • Provide mentoring and staff career development, encourage personal growth and foster good communication among team members
  • Supervision of team members/project teams as required
  • Pharmaceutical formulation development/R&D experience
  • Able to design, plan and conduct designed experiments to understand the impact of inert ingredients on development of new pharmaceutical drug product
  • Understanding of different types of drug dosage forms
  • Aware of analytical characterization of pharmaceutical products like drug release profile, in vitro in vivo correlation and understanding of bioequivalence studies
  • Aware of cGMP practices, ICH guidelines to manufacture quality products
  • Good mechanical aptitude in operating and troubleshooting laboratory equipment
  • Aware of working principles and preferred if have hands on experience of Tablet compression
  • Awareness about design of experiments
  • Strong communication skills to present research findings to R&D members
Apr 16th, 2019 11:07PM Apr 16th, 2019 11:07PM Health Care Pharmaceuticals & Biotechnology
9 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 16th, 2019 12:00AM Sr. Manager / Associate Director, Formulation Development Open Gen & Admin Boulder, CO, US Boulder CO USA Mar 1st, 2019 12:00AM

Company:

Array BioPharma Inc. is a fully-integrated, biopharmaceutical company headquartered in Boulder, Colorado. Array is focused on the discovery, development and commercialization of transformative and well-tolerated targeted small molecule drugs to treat patients afflicted with cancer and other high-burden diseases.

Summary:  Residing in our Boulder, CO office, this position provides technical support and oversight of formulation development, and drug product manufacturing.

Responsibilities:

Support Array sponsored external contract formulation and manufacturing partners including the following activities:

  • Leading formulation tasks or projects to meet the needs for new liquid or solid dosage form development
  • Actively participates in all the phases of development including the pre-formulation, process development, scale-up and support for the transfer to the pilot plant
  • Manage CMO’s for routine GMP production of drug products, including manufacturing, packaging, labeling, and distribution of clinical trial materials
  • Identify, evaluate, and qualify new CMO’s for GMP production of drug products
  • Contribute to studies and/or activities necessary for process optimization and continuous improvement to assure robust and cost-effective manufacturing processes
  • Assure consistent and reproducible manufacturing processes and final drug products
  • Support OOS, root cause, and CAPA investigations, as necessary
  • Manage and execute troubleshooting activities, as necessary
  • Transfer manufacturing operations to alternate sites, as appropriate, to assure continuity of supply
  • Write, review, and approve GMP batch records and protocols
  • Write RFPs, negotiate quotations, and verify invoices are consistent with work performed by CMO’s Work with Legal department to establish agreements and contracts with CMOs
  • Understand and practice good documentation practices in a GMP environment
  • Contribute to preparation and review of regulatory documents for submission to FDA and other regulatory authorities Identify and utilize expert consultants, when necessary
  • Follows Standard Operating Procedures (SOPs), protocols and other instructions from management
  • Execute and review experiment protocols, data summaries, reports
  • Draft or review SOPs, technical documents, analytical method validation protocols and reports
  • Takes a leading role in setting strategic department initiatives
  • Exercises judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results
  • Effectively uses the Array document management system including the change control module
  • Provide mentoring and staff career development, encourage personal growth and foster good communication among team members
  • Supervision of team members/project teams as required
  • Pharmaceutical formulation development/R&D experience
  • Able to design, plan and conduct designed experiments to understand the impact of inert ingredients on development of new pharmaceutical drug product
  • Understanding of different types of drug dosage forms
  • Aware of analytical characterization of pharmaceutical products like drug release profile, in vitro in vivo correlation and understanding of bioequivalence studies
  • Aware of cGMP practices, ICH guidelines to manufacture quality products
  • Good mechanical aptitude in operating and troubleshooting laboratory equipment
  • Aware of working principles and preferred if have hands on experience of Tablet compression
  • Awareness about design of experiments
  • Strong communication skills to present research findings to R&D members
Apr 15th, 2019 11:06PM Apr 15th, 2019 11:06PM Health Care Pharmaceuticals & Biotechnology
10 nasdaq:arry www.arraybiopharma.com www.arraybiopharma.com Apr 17th, 2019 12:00AM Commercial Analytics, Analyst / Manager Open Commercial Boulder, CO, US Boulder CO USA Mar 21st, 2019 12:00AM

Company:

Array BioPharma is a biopharmaceutical company headquartered in Boulder, Colorado that is focused on the discovery, development and commercialization of targeted small molecule drugs to treat patients afflicted with cancer.  Array recently received approval and launched BRAFTOVI (encorafenib) and MEKTOVI (binimetinib) for the treatment of patients with BRAF mutated melanoma. These products have also been granted Breakthrough Therapy Designation by the FDA for BRAF mutated CRC. 

 This position will reside in Boulder.

Responsibilities:

  • Provide analytic support to enhance the business strategies and tactical execution
    • Assist with analytics for the portfolio including tracking account performance, GPO performance, and providing insight into short term forecasting
    • Design and conduct quantitative analytics and modeling on secondary data (such as third party claims, GPO, Specialty Pharmacy, or IQVIA DDD/Xponent) to address business questions
    • Provide an objective commercial viewpoint based on an in-depth understanding and analysis of commercial performance
    • Help track KPI attainment and develop implications on short-term forecasting and sales trends.  Develop and issue regular performance update reports to senior management.
    • Assist in tracking payer insights including payer mix and formulary coverage among key payers
    • Track effectiveness of tactical initiatives to inform future activities
  • Step outside core responsibilities to help the organization frame and solve complex problems where needs arise
  • May design and conduct both qualitative and quantitative market research with vendors, analyze results, and report out key insights with strategic recommendations
  • Develop presentations with clear storylines, communicating key insights and recommendations while integrating data sources and existing team knowledge
Apr 16th, 2019 11:07PM Apr 16th, 2019 11:07PM Health Care Pharmaceuticals & Biotechnology

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