HemeClinicalTrialRMAM(m/f/d)

The 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 * 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 **Basic Qualification** * Advanced degree in medicine, pharmacy, life sciences or related field (MD, PharmD, PhD or equivalent). * At least 3 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 woul