…Unit physicians, Outcome Liaisons, Medical Information). + Collaborate with US Medical Affairs , Regulatory , Legal, or other departments and external experts +

…Unit physicians, Outcome Liaisons, Medical Information). + Collaborate with US Medical Affairs , Regulatory , Legal, or other departments and external experts +

…of Investigator Initiated Studies + The CL-EP works with the Global Labeling Teams, Regulatory Affairs and Safety to update the Core Date Sheets, EU, US

…databases. This individual will partner closely with clinical research managers, regulatory affairs managers, quality specialists, and biostatisticians to

…collaborations with project leaders and projects team members, including biostatistics, regulatory affairs , clinical pharmacology, genetics, PM, and development

…globally + Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval. + Studies must

…operations. + Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval. + Studies must

…(HR), Plant Engineering, Facilities Design & Construction (FD & C), Accreditation Safety and Regulatory Affairs (ASRA) , and others as needed for consultation on

…other departments, including but not limited to Clinical, Quality, Medical Safety and Medical Affairs and Regulatory Affairs to ensure program execution to

…Research partners andcross-functional partners (eg Global Strategic Marketing, MedicalAffairs, Regulatory Affairs , R&D, etc.), ensuring alignment. +