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Provide practical and timely legal guidance on issues related to clinical, biometric, medical affairs, patient advocacy, regulatory affairs, pharmacovigilance, program and asset management, commercial development, pricing & reimbursement, sales, marketing, market access, patient services, and government affairs.
$306,700 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Sr. Director, Biostatistics and Statistical Programming, is accountable to the Chief Medical Officer and Head of Biometrics for ensuring the statistical strategy and the integrity and quality of data deliverables to meet program-level objectives, regulatory requirements, pharmacovigilance data review and medical affairs.
$361,400 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Job Title: Regulatory Affairs Manager (Retail Energy + Wholesale Market in OH, IL, PA, MI) At least 7-10 years of prior working experience in regulatory affairs, policy advocacy, governmental licensing and permit processes in a retail and wholesale energy business setting.
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The Clinical Research Regulatory Specialist is expected to facilitate the development of grant and clinical trial submission of applications and annual reports, development/maintenance of study-specific case report forms and source document tools, provide direct regulatory/compliance guidance, and facilitate investigator-initiated multi-site trials—additional duties relevant to regulatory affairs as assigned.
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Experience in other Medical Affairs functions (i.e., Publication Planning, Scientific communications, HEOR, etc.) Inizio Engage has a strong partnership with an emerging biopharmaceutical company in endocrinology/rare disease to support Medical Affairs activities and execution.
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Develop and lead comprehensive external relations and government affairs strategies to build and nurture relationships with US government bodies, policymakers, and regulatory agencies, and leverage these relationships to shape policies that align with IDP’s mission and growth goals.
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The director will work closely with GSK Public Policy & Government Affairs as a thought partner on market access implications of proposed policy issues to shape the health policy environment and advance GSK’s policy agenda and will also be responsible for leading teams in price negotiations with state and federal regulators.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
$2,039 a weekFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As an Anti-Money Laundering ("AML") Project Associate (Senior Consultant), you will have the opportunity to help our clients mitigate their risks related to money laundering, terrorist financing , and sanctions violations, as well as to improve their ability to meet regulatory requirements, expectations , and guidance in support of developing and maintaining sound AML and sanctions programs and controls.
$162,800 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Associate Director – CMC Regulatory is responsible for leading global CMC regulatory activities for Lilly/Avid diagnostic radiopharmaceutical products. Review technical documents including testing protocols, technical reports, and CMO procedures and specifications from a CMC regulatory perspective.
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PHMC is proud to be a leader in public health.
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Reporting to Jefferson’s Central Region Chief Clinical Officer (CCO), the CMO/CQO is an integral member of the TJUH hospitals leadership team providing oversight and leadership on Medical Staff Activities & Affairs, Regulatory Affairs, Quality and Safety, and Clinical Development and Operations.
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CCRP - Cert Clin Research Prof (Preferred) or RAC - Regulatory Affairs Cert (Preferred) 2 Years experience in a regulatory role or 4 Years experience in related clinical research role (Required.
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In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
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Contribute to the firm’s regulatory obligations, including analysis of existing and new regulations and testing the effectiveness of the broker-dealer compliance program. Review marketing materials for compliance with relevant regulatory standards (SEC, FINRA, etc.
$85,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago
regulatory affairs jobs Title: reimbursement in Philadelphia, Columbia, Missouri
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