Job Description: Oxford Global Resources is looking for a Medical Project Manager in Madrid who will be joining a research-based bio pharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet medical need. Client's therapeutic areas of focus include liver diseases, infectious diseases, and hemato-oncology. We are seeking a knowledgeable and motivated professional with a high capacity for adaptation to different therapeutic areas and medical affairs roles. Close collaboration with National and International colleagues within Medical Affairs and cross-functional collaboration will be required.
The position will be based in Madrid and will report to the Medical Director.
Responsibilities:Develop and execute Medical Affairs plan, in close collaboration with other medical team members.Work collaboratively with personnel in European affiliates, Global Medical Affairs, Clinical Research, Marketing, Market Access, Sales, Regulatory Affairs, Drug Safety, Public and Government Affairs.Provide local medical expert input into global product development teams.Work with the cross-functional brand and launch team.Serve as internal scientific expert in the therapy area, healthcare landscape.Represent the company with experts, medical professional groups, societies, patient representatives, regulatory groups, and at national and international scientific meetings.Establish and maintain strong working partnerships with external medical experts locally and internationally, including academic societies.Conduct meaningful scientific exchange and communicate complex scientific information and data in an organized and fair/balanced manner while demonstrating judgment and integrity in accordance with the highest ethical and compliance standards, including the company's Code of Ethics and Business Conduct policies, and applicable legal and regulatory requirements.Plan and conduct Advisory Boards as needed to obtain insights.Develop and conduct medical education and communication activities, including digital, face-to-face, and print.Support the generation of scientific data through collaboration with Gilead personnel in R&D; and Clinical Operations, site support in clinical trials, and by developing local clinical trials including study protocols, as needed.Assist investigators with submission of investigator-sponsored studies, following up the review and approval process and the publication plan.Education:Advanced scientific degree (i.e., MD, Pharmacy, PhD).5-6 years experience in medical affairs.Good knowledge of the Spanish National Health System environment.High ability to adapt to different therapeutic areas and medical affairs roles.Demonstrated ability to lead change through thinking strategically to drive innovation.Demonstrated relational intelligence by generating value through impactful interactions.
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