Affairs, Oncology Business Unit (OBU) will provide and drive near and long-term strategic direction, as well as development... and implementation of medical affairs research strategies (including post-approval investigator-initiated research, phase 3b/4...
Head of Ethics & Compliance (E&C) for PDT R&D and Medical Affairs at the senior director level is a senior leader... of regulatory trends. Reporting to the Head of E&C for PDT, this leader collaborates across global E&C teams and PDT stakeholders...
such as Pharmacovigilance/Safety, Quality, Legal, Regulatory Affairs, Commercial, Clinical Operations, Clinical Development, and Information... activities. In partnership with Northeastern University, Alnylam Pharmaceuticals is offering a two-year Global Medical...
Evidence Generation Medical Affairs Operations Health Economics and Outcomes Research (HEOR) Global Regulatory Affairs... educational needs. Congress Strategy and Execution Gain hands on experience in supporting medical affairs presence at global...
-functional teams, including R&D, external manufacturing, quality control, vendor quality and regulatory affairs, to align...Job Description Job Posting Description As the Associate Director of Strategic Sourcing, you will be a part...
underserved therapeutic areas and make patients the focus of every strategic decision. Role Summary The Senior Director... Senior Director, Patient Advocacy will lead strategic collaborations with patient advocacy organizations and patient...
Regulatory Affairs, and external CRO partners to ensure timely, high-quality execution of clinical trial agreements and budget... The Director, Clinical Trial Contracts and Budgets, is responsible for building and leading a high-performing team...
Affairs, Regulatory, Legal, Development Quality, and other internal partners. Manage external vendor performance, including...-functional and vendor relationships Strong working knowledge of ICH-GCP, global regulatory requirements, and local trial...
Affairs, Regulatory, Legal, Development Quality, and other internal partners. Manage external vendor performance, including...-functional and vendor relationships Strong working knowledge of ICH-GCP, global regulatory requirements, and local trial...
Job Description General Summary: Vertex Pharmaceuticals is seeking an Associate Director (AD) of Kidney Field... Training & Development to join the North America Commercial Field Training (NACFT) organization. Reporting to the Director...
The Medical Director (Clinical Development, Regulatory and Safety), will hold an expert position within the Amyloidosis... pharmacology, translational medicine, regulatory, biostatistics, safety, CMC, medical affairs, and commercial partners. Analyze...
or pharmacovigilance audit program, hosting/leading regulatory inspections, investigations and remediation activities on a global level... Associate Director, Clinical & Quality Process Compliance is responsible for ensuring the quality of processes and product...
Regulatory Affairs (RA) representative for assigned products. They will be responsible for reviewing and approving the regulatory... content of materials created for product promotion, disease awareness and public affairs communications. The Director...
Job Description General Summary: The Clinical Development Medical Director will serve as the Medical Lead... to achieve efficient, high-quality study execution Participates in the preparation of regulatory documents in support...
community and will provide medical expertise to support regulatory submissions and interactions with global regulatory... and modest costs. Description of Role The Senior Director, Clinical Development will play a leadership role in Centessa...
stakeholders across the CVRM Global Franchise, Global Corporate Affairs, Global Medical Affairs, Investor Relations and research... at a leading multinational biopharma company or at a global agency, backed up by deep understanding of regulatory environment...
· Interact cross-functionally with Commercial, Medical Affairs, Drug Safety, Regulatory, Legal, Compliance and Finance to develop... not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your role: As the Director Field...
regulatory teams and external partners to deliver global submissions and maintain compliance under design control... with diagnostic companies. Hands-on experience with global regulatory pathways (FDA IDE/PMA; EU IVDR CPS/performance requirements...
regulatory teams and external partners to deliver global submissions and maintain compliance under design control... with diagnostic companies. Hands-on experience with global regulatory pathways (FDA IDE/PMA; EU IVDR CPS/performance requirements...
. Collaborate with Global Project Heads, Clinical Research Director, Safety Officer and Pharmacovigilance, Translational Medicine..., Regulatory Affairs, Biostatistics, Clinical Study Units, Medical Affairs, and CROs to optimize study design and execution...