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15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
$113 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The candidate should have over 12 years of experience in pharmaceutical/biotech drug development, including more than 4 years in global CMC regulatory affairs, with expertise in PDM development for NCEs/small molecules.
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The Community Choice Financial Family of Brands is currently seeking a Deputy General Counsel- Regulatory. Deputy General Counsel - Regulatory. Reporting to the Chief Legal Officer, the DGC is responsible for managing a diverse array of consumer lending regulatory matters, general legal matters involving privacy, corporate governance, finance, and legal operations issues, as well as, contracts, and assisting in developing and managing a team of highly talented legal professionals.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Provide regulatory guidance to PI's and Research Staff to support the successful submission of regulatory compliant materials that are approved by the IRB or IACUC as applicable. Review all IRB and/or IACUC submissions to verify the required documents include all necessary information to make regulatory decisions.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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The US GRPA team is responsible for monitoring new developments impacting the US prudential regulatory capital regime, as administered by the US Agencies - the Federal Reserve, OCC, and FDIC. Strong technical working knowledge of the prudential regulatory capital rules relating to the calculation of regulatory capital resources, RWAs, and the leverage ratio; knowledge of these concepts under US (Fed / OCC / FDIC) rules is essential.
$235,900 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Join Arkema in Wauwatosa, USA, as a Product Stewardship and Regulatory Affairs Specialist. If you are a driven individual with an interest in regulatory affairs and product stewardship, apply now.
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Reporting to the One Medical Assistant General Counsel - Clinical and Regulatory, the Corporate Counsel will support our company’s clinical and regulatory matters, as well as be a key adviser to One Medical’s clinicians and operations team.
$258,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collaborate with onshore teams and stakeholders to gather business requirements related to QMS functionalities, with a focus on Post Market Surveillance, Complaints Management, CAPA, Nonconformance, and Regulatory Submissions.
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Partner with Drug Metabolism and Pharmacokinetic (DMPK) and Bioanalytical (BA) Subject Matter Experts (SMEs) to author, review and track regulatory documents. Understand the impact of DMPK/BA and interdependencies with other functional teams within the enterprise including Pharmacology, Toxicology, Clinical and Regulatory disciplines.
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Quality and Regulatory Affairs Specialist. The Quality and Regulatory Specialist facilitates and participates in the implementation of the multidisciplinary hospital and system wide Clinical Quality and Patient Safety Performance Improvement Program.
$131,538 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Assist with quality review of DMPK reports that are generated by DMPK scientists by fully reviewing the raw data outputs/electronic notebooks and ensuring validity and quality of reported data in the reports, in addition to reviewing DMPK regulatory documents, editing of nonclinical study reports for regulatory acceptance and adherence to company templates, SOPs, DMPK/BA methods, work practices and FDA GLPs, as applicable.
$57 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Innova Solutions is immediately hiring for a Nonclinical Regulatory Document and Scientific Writer. Assist in addressing Health Authority questions pertaining to DMPK and BA with the SMEs and Regulatory representatives.
$58 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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You'll gain insights into our Compliance function through an immersive program, starting with comprehensive training and progressing to team-based work in areas like Financial Services Compliance, Anti-Money Laundering, Client Onboarding, Trade Account Operations, Enterprise Risk Management, and Regulatory Strategy.
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Bachelor's degree in Environmental Science, Physical Science, Land Management, Regulatory Affairs, or a related field preferred. At least 2-5 years of experience in regulatory compliance or environmental permitting within the oil & gas industry, with specific experience in Salt Water Disposal wells and water recycling preferred.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Collaborate with key stakeholders across the organization, including clinical operations, regulatory affairs, data management, and IT, to assess user needs, gather requirements, and develop tailored solutions to address business challenges.
$45 an hourExpandApply NowActive JobUpdated Today
regulatory job Title: regulatory affairs Company: Pwc
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