Senior Heme Clinical Trial RMAM (m/f/d)

The Senior Heme Clinical Trial RMAM is responsible for the successful conduction of all our clinical trials in Germany and is responsible for efficient and compliant management of medical and scientific study activities to generate robust evidence that supports the scientific positioning and the medical care of patients.

Requirements

• Lead and coordinate medical research activities on a local level to ensure high scientific and operational quality
• Ensure that all clinical studies are planned, executed and communicated in line with regulatory standards and company objectives
• Manage internal and external partners to ensure quality, timelines and budget are met
• Develop regional omnichannel engagement plans, combining face-to-face and digital outreach to meet healthcare professional needs.
• Acting as a central interface between local and global Medical Affairs stakeholders, regional medical affairs managers, clinical development and clinical research organizations to ensure cross-functional collaboration
• Plan and run regional medical activities such as advisory boards, symposia and educational meetings.
• Contributes to the generation of high-impact and robust data in clinical trials to inform treatment decisions, support product differentiation and improve outcomes for oncology patients
• Mentor and support development of more junior medical colleagues.

Benefits

• Competitive salary and benefits package
• Opportunity to work with a global biopharma company
• Collaborative and inclusive work environment