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Leads the execution of global CMC regulatory plans, including overseeing the submission preparation process in close partnership with other functions in PDM, Regulatory Affairs, and Clinical Development.
$307,560Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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As a Director, Global Regulatory Affairs, Precision Medicine you will develop and execute Precision Medicine regulatory strategies in alignment with the drug global regulatory strategy in collaboration with cross functional stakeholders across the Gilead therapeutic areas and in compliance with the appropriate regulations.
$266,200 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Business Operational Excellence function works across Gilead Global Regulatory Affairs (GRA) to provide the framework for GRA process development and excellence, controlled documentation development and management and effective learning programs.
$307,560 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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In this role, you will be responsible for strengthening of awareness, affinity, and leadership of the Zoox brand, leading Public Relations, Media Relations, Public Affairs, Corporate Social Responsibility, Crisis Communications, Analyst Relations, and Event Activations.
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The Manager of Medical Affairs reports to the Senior Director of Medical Affairs and will support the Medical and Scientific Affairs teams with operational and organizational needs related to vendor contracts, HCP consulting agreements, work orders for HCPs and vendors, POs, invoices, and related financial forms.
$72 an hourExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Associate Director - Strategic Operations, Global Medical Affairs, Oncology. We have an exciting opportunity on our Medical Affairs Team, an Associate Director position within Global Medical Affairs Oncology.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Provide guidance and support to R&D scientists on histology techniques and uphold laboratory safety and regulatory compliance. Familiarity with regulatory compliance and LIS systems. Certification as a Histotechnician (HT) or Histotechnologist (HTL) by the American Society for Clinical Pathology (ASCP) required.
$50 an hourExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Oversee samples management logistics for clinical and non-clinical samples, ensuring compliance with protocols. The Pathobiology Lab Operations Group at Gilead Sciences is seeking an experienced Histology Technician to enhance our pathology and translational research efforts.
$52.67 an hourFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Expertise in statistical methods to support medical and scientific affairs including analysis using the clinical database for scientific meetings, publications, and internal decision-making (generally based on previously conducted randomized clinical trials.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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In partnership with Clinical Research, Medical Affairs and Development functions, ensures that all clinical trial activities are performed in accordance with all applicable SOPs, company policies and regulatory guidelines to provide timely delivery of high quality clinical data to support global registration and commercialization of Gilead's products.
$168,520 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Working to ensure all clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data, that supports global registration and commercialization of Client’s products.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Infrastructure Architecture – Design and implement scalable, secure, and highly available Cloud infrastructure solutions on Microsoft Azure; Collaborate with cross-functional teams to gather requirements and translate them into robust and efficient architecture designs; Ensure Compliance with industry best practices, security standards, and regulatory requirements.
ExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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Regulatory Affairs CMC – Data Administrator Contractor. § Work is performed under the general supervision of more senior Regulatory Affairs CMC Systems professionals. Regulatory Affairs CMC – Data Administrator Contractor.
$70 an hourExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Should have experience with Veeva Vaults, experience with the RIM Vault preferred. Perform data entry using Gilead Information Systems to enter and maintain relevant product information to support cross-functional stakeholders.
$55 an hourExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The Pathobiology Lab Operations Group at clients Sciences is seeking an experienced Histology Technician to enhance our pathology and translational research efforts. The ideal candidate will bring advanced expertise in histological procedures, including tissue processing, staining techniques, and digital pathology, to support our drug development pipeline.
Full-timeExpandApply NowActive JobUpdated 12 days ago
regulatory affairs jobs Title: clinical director in Foster City, East-hartford, Connecticut
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