Company: Regeneron Pharmaceuticals

The Associate Director, Senior Medical Advisor assists in the development of medical strategy, planning, and execution of oncology-related medical affairs activities at Regeneron UK. This hire provides scientific and/or medical expertise by thoroughly understanding oncology, particularly immuno-oncology, and serves as a scientific/medical resource. The Associate Director will work in a multifunctional, matrix organization, closely collaborating [...]Read More... from Associate Director, Medical Advisor (Oncology) See details

The Program Data Management Lead is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management activities and decisions including quality, timelines and resources related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures [...]Read More... from Associate Director, Program Clinical Data Management Lead See details

The Manager Statistical Programming provides timely support to the study team on all programming matters according to the project strategies. Provide project leadership and programming support for processing data from clinical studies. Provides guidance in implementing and performing the programming and project standards. Lead the programming aspect of a project, both internally or CROs, for [...]Read More... from Manager, Statistical Programming See details

We are seeking a dynamic and dedicated Commercial Project Manager – Training and Operations to join our International Oncology team. This role is pivotal in supporting Commercial Training and other Commercial Operations deliverables across multiple geographies outside of the US. You will work closely with cross-functional stakeholders, including Comm Ops, Marketing, Medical Affairs, and Comm [...]Read More... from Commercial Project manager – Training and Operations See details

The Senior Clinical Study Lead (CSL) is expected to operate with a high degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close-out. The Senior CSL is accountable for the study timelines, study budget, and ensuring study conduct is in [...]Read More... from Senior Manager, Clinical Study Lead See details