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Collaborating with Global Clinical Supply Chain functions and external Vendors on the package design and label development for investigational product to meet all protocol and regulatory requirements.
$78 an hourExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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This position reports to the VP, Global Regulatory Affairs. Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific merits of Chemistry, Manufacturing and Control (CMC) and nonclinical study data package.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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The Senior Director of Clinical Development Medical Affairs (CDMA) oversees the strategic planning and execution of our nitric oxide program, ensuring alignment with brand objectives, incorporation of insights, and the development of an R&D plan addressing unmet patient needs and competitive differentiation.
$255,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Minimum 5 years in Regulatory Affairs, including leadership roles. Ensure effective execution for new innovative consumer-centric products and the life cycle management of products in the portfolio across the following regulatory classes (OTC monograph drugs, dietary supplements, cosmetics, foods and medical devices.
$95.7 - $110.7ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Job Title: PV Liaison Senior Manager (USA), Regulatory affairs Location: Candidate must go to NJ, Bridgewater office 2-3 times a week. Responsibilities PV Liaison Senior Manager (USA): o Supports the CSH in all PV related activities at the country level, including but not limited to management of cases, periodic safety reports, activities of local vendor, safety surveillance of marketed products, audits / inspections, compliance of Local Pharmacovigilance, PV Regulatory Intelligence and PV awareness training.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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G&L Healthcare Advisors is a specialist provider of consultants to the healthcare industry for all aspects of Regulatory Affairs, Quality Assurance and Clinical support. A good understanding of the Regulatory Affairs and Quality Assurance fields.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Pharmaceutical Regulatory Affairs Senior Manager will use their experience and knowledge in pharmaceutical industry regulatory affairs to lead and manage complex projects for our clients in the pharmaceutical sector, and provide strategic advice, guidance, and solutions on regulatory matters.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams, including engineering, marketing, and regulatory affairs, to gather and prioritize requirements for digital services. Ability to navigate complex regulatory environments.
Full-timeExpandApply NowActive JobUpdated 5 months ago
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