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

Position Overview

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.

Responsibilities

• 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
• Act 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
• Contribute 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 the development of more junior medical colleagues

Basic Qualification

• Advanced degree in medicine, pharmacy, life sciences or related field (MD, PharmD, PhD or equivalent)
• At least 5 years experience in medical affairs, medical science liaison, clinical research or related industry role
• Strong clinical and scientific knowledge relevant to the therapy area for the role
• Excellent verbal and written communication skills in German and English
• Willingness and ability to travel regularly within the assigned region
• Solid understanding of regulatory, ethical and compliance requirements in the pharmaceutical environment

Preferred Qualification

• Prior experience in oncology, hematology or related therapy areas
• Experience supporting investigator‑initiated trials or clinical partnerships
• Experience designing or delivering omnichannel engagement plans and digital medical communications
• Project management or budget management experience
• Experience presenting at national or regional scientific meetings
• A collaborative mindset and commitment to inclusive working with diverse stakeholders

Equal Opportunity Employer

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to ethnicity, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.