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Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities. The key functions of this role will be to collaborate with internal and external stakeholders including the Foster City Medical Affairs team, Scientific Publications, Medical Affairs Research, Marketing, Global Commercial Product Strategy, Value and Market Access, Clinical Research, Public Affairs, Government Affairs, Contracts/Finance, Pharmacology, Virology and Legal on both the global and regional levels.
$55 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Serve as USMA Head of HIV Treatment in cross-functional meetings, representing the US perspective and needs in working groups with Clinical Development, Global Medical Affairs, US Commercial, US Government Affairs and Policy, US Public Affairs, US Regulatory, and US legal and compliance.
$441,540 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Ensure that each group has appropriate protocols to support tech transfer including process development, QA/QC, and regulatory. Experience interacting with government regulatory agencies is a plus (FDA, DEA, etc.
$285,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The optimal candidate participate will lead the department and also collaboratively work across a team of peers in Clinical, Regulatory, Biometrics, Medical Affairs and Commercial and will be accountable for ensuring safety systems, staff and procedures are in place to support a compliant global pharmacovigilance system.
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This role will oversee the development and implementation of statistical programming strategies, manage a team of statistical programmers, and collaborate closely with cross-functional teams to ensure high-quality deliverables that meet regulatory requirements and support drug development efforts.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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LocationsStanford Health CareWhat you will doGuarantees adherence to manufacturer guidelines, SHC regulatory compliance, and local, state, and federal regulations for Acute Dialysis services, maintaining treatment integrity and safety.
$55.8 - $73.92 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Engineering Documentation Manager will be responsible for responsible for the day-to-day management of the Change Analyst Process to ensure documentation and engineering changes meet applicable customer, regulatory, and company requirements.
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Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
$36.54 an hourFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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A law firm in Redwood City, CA, is seeking a CFIUS and International Trade/Export Controls Associate Attorney with 2-4 years of experience in handling international trade regulatory matters, compliance, and enforcement.
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Senior Regulatory Affairs Manager (Open to Remote, Hybrid and Onsite Options) Full-time. 5+ years experience in a medical device or IVD regulatory affairs role, preferably in molecular diagnostics.
$177,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This investigation includes but is not limited to a criminal, civil litigations and regulatory review, employment, education, and credit review (role dependent). We assist companies and non-profit organizations in delivering benefits to their employees.
$75,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Work collaboratively with Manufacturing, QA and Regulatory to support CMC analytical deliverables. Hands-on experience with a wide range of analytical techniques such as ELISA, SDS-PAGE, Western Blot, Karl Fisher and HPLC (SEC, IEX, HIC, RP, affinity.
$162,046 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Author/review and/or coach team members to author CMC regulatory sections of IND/INDa. Contribute to regulatory strategies and support associated agency interactions and product-related inspections.
$247,610ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Contribute to corporate strategy for inspection preparation or additional regulatory approval relating to Exact Sciences histopathology. ASCP Board of Certification, to include Histotechnician (HT) American Society for Clinical Pathology (ASCP), or Histotechnologist (HTL) ASCP.
$131,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines in support of investigational studies.
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regulatory affairs jobs Company: Citi in Menlo Park, CA
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