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

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About the role

The Senior Hematology Clinical Trial Senior Hematology Clinical Trial (Regional Medical Affairs Manager/RMAM) (m/f/d) 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). • Multiple 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-GSK #LI-Remote Skills Digital Fluency, Enterprise Thinking, External Stakeholder Management, High Impact Communication, Patient Journey     Germany Salary Range / Gehaltsbandbreiten Deutschland: EUR 98,250 to EUR 163,750The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets

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