As our Medical Science Liaison (MSL), you’ll be part of our field-based medical team, reporting to the MSL National Field Director, acting as an extension of the Medical Affairs team. You’ll serve as a key scientific resource and expert on cell therapy for both health care professionals (HCPs) and internal stakeholders. Domestic travel of approximately 50-70% will be required.
As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will assume responsibility for an individual project, or many projects and communicate in an optimal way, making sure that specific client objectives are met. Responsible for the set-up and maintenance of the project(s).
The Drug Safety Physician will be responsible for the pharmacovigilance function, including medical review and oversight of processing for all types of safety events. The individual will provide clinical support of drug safety data management and interpretation and risk management activities for the company. This includes oversight of clinical trial Serious Adverse Event (SAE) processing and safety data analysis to support signal detection and risk/benefit profile evaluation.
As a Medical Director, you will lead the clinical sub-team or support it and the global program team to build global clinical development plans and contributes to the development of asset level and therapeutic area strategies. You will be responsible for overseeing the clinical development strategy development and execution for 1 program, leading the clinical subteam, contributing to the development of regulatory strategy, and representing the clinical program at regulatory meetings