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. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Lead and coordinate medical research activities on a local level to ensure high scientific and operational quality Ensures 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. 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 If you have the following characteristics, it would be a plus: 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. Weitere Informationen: Annual Report Product Pipeline #EBDE #LI-ViiV #LI-Remote Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. 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