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Associate Director-Diabetes & Obesity Biology
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This position will work closely with the Technical Operations (CMC) functional groups and Regulatory Affairs department to plan and author high quality regulatory submissions to health authorities and will have frequent interaction with internal senior management, corporate partners, international regulators and external experts.
$329,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collaborate with all Airport Divisions, including Operations, Design & Construction, Sustainability, Facilities, Business & Finance, External Affairs, People, Performance & Development, and Strategy & Social Impact.
$206,206 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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5 - 7 years of experience in Regulatory Affairs or a related discipline in the pharmaceutical or healthcare industry (preferably with exposure to document control systems) The Manager of Regulatory Affairs will focus on managing regulatory documentation for the 4DMT programs.
$145,000 a yearExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This is a highly collaborative role and will work closely with The Customer Service, Clinical Operations, Provider Network Operations and Compliance and Regulatory Affairs Departments. Present grievance and appeals data to key stakeholders through Grievance Review Committee (GRC) and the Grievance Program Leadership Team (GPLT) as needed.
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Mammoth is hiring aDirector/Sr. Director, Regulatory Affairs, Therapeutics, to lead the regulatory activities of our growing CRISPR-based therapeutic programs as we bring them from concept to market.
$260,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work in close cross-functional collaboration with Clinical Operations, Regulatory Affairs, Program Management, Quality Assurance, Biometrics and Data Management, Pharmacovigilance and Clinical Research Organizations (CROs.
$240,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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As the MSL reporting to the Director of Medical Affairs, you will serve as a central conduit between Olema and the breast cancer medical community. Develop and fulfill a territory plan in collaboration with Medical Affairs customers that is designed to support shared business objectives and complete gap analysis to optimize impact in field.
$220,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The successful candidate will oversee and direct all Quality Unit functions (QA, QC and Quality Systems) and collaborate with internal business partners (including Manufacturing, Supply Chain, Process Development, Regulatory Affairs) to deliver the innovation pipeline and meet business targets.
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Lead early and late-stage drug product development activities including scale-up, design of experiments (DOEs), risk assessments, and development of the integrated control strategy in partnership with other CMC functional areas, Quality, Regulatory Affairs, and Manufacturing.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Identify laboratories to publish abstracts working with Scientific Affairs in support of Hologic Diagnostic products and product launches. Minimum of 3 years related experience as Cytotechnologist, or 1-year experience with a master’s degree in gyn and non gyn cytology as Cytotechnologist.
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Collaborate with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Clinical Research, Quality Assurance, Global Patient Safety and Risk Management, and Regulatory Affairs; CROs, central and local laboratories, and other vendors.
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12+ years of legal experience as an attorney, including experience at an established law firm and in-house at entertainment/media companies, with 8+ years of extensive experience negotiating and drafting a wide range of entertainment-related agreements and 3+ years of legal experience in a business and legal affairs role focusing on original scripted series content production.
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Safety Statisticians are part of collaborative, cross functional teams including members from Pharmacovigilance and Patient Safety and Epidemiology (e.g., product safety team physicians, epidemiologists, safety analysts), Statistical Programming, Clinical Statistics, Regulatory Affairs, and Medical Writing.
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Prior experience in thought leader engagement, regional marketing, sales, medical affairs, or sales leadership. Work closely with sales, marketing, and medical affairs teams to ensure alignment with conference engagement plans.
$218,348 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
affairs job Company: Biophase in San Francisco, CA
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