Overview Descripción del trabajo Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well‑being of people around the world. We are leaders in plasma‑derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment. Responsibilities As a Global Medical Affairs Manager, build partnerships with external healthcare professionals and internal stakeholders to communicate evidence based scientific, technical and development information related to Grifols biopharma products and therapeutic areas. Execute Global Medical Affairs Plan Execute and participate in the development of global medical affairs plans, guided by a senior colleague. KOL Engagement — Build and maintain relationships with relevant key opinion leaders globally. Provide subject matter expertise and insights in the therapeutic area. Knowledge management in the respective area, acting as a subject matter expert, participating in internal education, preparing medical content and writing summaries when needed. Gather insights from KOLs, congresses, competitor information, etc., to inform medical strategy and innovation. Attend relevant international congresses in the area of responsibility. Coordinate congress planning, organize F2F KOL meetings, and prepare congress reports. Contribute to presentations to internal stakeholders. Collaborate in the execution of advisory boards or expert meetings. Disseminate data to the medical community and other key stakeholders. Collaborate in the execution of international scientific events such as symposia, webinars or standalone meetings. Support Medical Information department on the review of standard response documents (SRD) for external customers. Contribute to scientific publications generated from Grifols MA projects or studies (including abstract writing or revision of manuscripts). Review the accuracy of medical content in global marketing materials. Medical function in the sign off process of promotional materials. Support Medical Affairs research programs such as global ISRs, RWE, NIS, Scientific Awards and research grants, following internal processes, guided by senior colleagues. Provide medical expertise and scientific input to cross‑functional partners. Collaborate with cross functional teams within the Scientific Innovation Office (SIO). Support commercial activities with subject matter expertise. Provide medical input in the development of value dossiers or other materials requested for reimbursement / market access support. Attend periodic cross‑functional team meetings on TA updates and strategy alignment. Manage projects and budgets, ensuring compliance Monitor and manage assigned project budgets, ensuring accurate tracking of expenditures and adherence to Grifols’ financial processes and compliance requirements. Work Interactions — Close cooperation with key influencers in the respective areas. Strategic partner of global marketing and the SIO. Close cooperation and strategic partner with commercial. Who you are To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and / or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions). Education University degree in Biology, Biomedicine, Biochemistry, Biotechnology, Pharmacy or Medicine. PhD, MD or PharmD with advanced knowledge in the immunology / neurology scientific field is preferred. Experience At least 2 years of experience in a similar position in the pharma industry preferably. Solid knowledge of medical / pharmaceutical basics with highest ethical standards. Scientific understanding (literature, clinical and basic research etc.) Skills Advanced communication and relation building skills Good English language skills (spoken and written) Willingness to travel What we offer It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply! We look forward to receiving your application! Grifols is an equal opportunity employer. Benefits Package Flexibility for U Program : Hybrid Model Flexible schedule : Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). Nature of Role : Individual Contributor Contract of Employment : Permanent position We remove tracking IDs and site-only notices to ensure clarity and alignment with formatting standards. J-18808-Ljbffr