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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.
$116,000 - $145,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead the migration of existing regulatory documentation to the new Veeva system. The role involves working closely with the regulatory information management vendor (Veeva) to lead the implementation of the Veeva RIM cloud-based software solution.
$116,000 - $145,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Partnering and aligning with Discovery, Regulatory, Operations, Quality, and Clinical functions, and managing CMC-focused deliverables and timelines to move programs from lab to the clinic and beyond.
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Review label claim documentation, quality certifications, specifications, plant audit reports, certificates of insurance and other legal or regulatory documents and present findings to the GO Brands Product Director and Director of Technical Services.
$85,000 - $105,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Proficiency in aseptic techniques and closed system processing with a solid understanding of GMP, FDA, and other regulatory requirements related to gene therapy manufacturi. ce:Ensure all manufacturing activities comply with Good Manufacturing Practices (GMP) and relevant regulatory requiremen.
$46 - $63 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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3+ years of drug development or medical or scientific affairs experience or equivalent clinical research experience at CRO or academic institution. Assists in writing clinical documents and amendments (clinical study protocols, Investigator's brochure, ICF template) and in the preparation of clinical content for regulatory submissions/documents, in collaboration with other clinical team members.
$150ExpandUpdated Yesterday - UpvoteDownvoteShare Job
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The ideal candidate for this role will possess a deep understanding of the digital asset business, encompassing trade lifecycle workflows, financing and risk operations, collateral management, liquidity management, and regulatory reporting.
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Essential Responsibilities:Provides high quality clinical supervision per California Board requirements (Board of Behavioral Sciences or Board of Psychology) covering all aspects of the student/intern/Associate/licensed providers (any supervisee) role including clinical documentation, treatment planning, crisis response protocols, Kaiser Permanente clinical workflows.
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Current industry and regulatory standards, including CBC, NEC, and NFPA standards 70E, 70B, and NETA. Preparation of construction documents, including specifications, medium and low voltage power distribution, raceway layout, underground duct bank, lighting, grounding, control schematics, and connection diagrams.
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Traveling, Nationwide - Seeking Reservist Hospitalist Medical Director Join the Physician Partnership Where You Have A Voice Vituity's ownership model provides autonomy, local control, and a national system of support, so you can focus your attention where you want it to be - on your patients.
$250Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Clinical skills include but are not limited to: vital signs, provide wound care, performs catheterization, Point of Care Testing and phlebotomy. Provides clinical support, care coordination and direct case management including patient education, goal setting, self-management teaching and coaching.
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Cross-functional Collaboration: Collaborate with various departments (e.g., Quality Assurance, Regulatory Affairs, Manufacturing) to understand business needs and translate them into system requirements.
$230,000 - $241,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Subject to regulatory alcohol & drug testing, which includes testing for marijuana, pcp, amphetamines, cocaine & opioids. Must pass all FedEx Express & regulatory/statutory required background checks or security threat assessments.
$25.64 - $39.03 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Wärtsilä Energy Storage & Optimization (ES&O) is the leading global energy storage optimizer.
$117,306 - $217,854 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Demonstrated knowledge and expertise in drug product development, formulation development, process development, manufacturing, and regulatory CMC. Maintain awareness of regulatory CMC requirements.
$150ExpandApply NowActive JobUpdated Today
regulatory affairs jobs Title: director clinical in Emeryville, Troy, New York
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