Experteer Overview
As a Medical Affairs Scientist/MSR, you will cultivate scientific partnerships with local KOLs to support access and advocacy grounded in evidence. You will serve as the in-field medical expert for GU tumours and lead local medical-scientific plans that align with regional strategy. You’ll acquire field intelligence, facilitate collaborations, and disseminate data via medical-to-medical communications, while ensuring regulatory and scientific standards. This role offers cross-functional collaboration and the opportunity to shape local medical strategy and investigator engagement.

Compensaciones / Ventajas
• Build and maintain relationships with KOLs and scientific institutions to support medical leadership
• Serve as the in-field medical expert for GU tumours
• Gather and interpret field medical intelligence to identify investigators and collaboration opportunities
• Plan and execute local medical-scientific strategic plans and support country-level TA activities
• Attend scientific meetings and lead medical-to-medical communications
• Prepare scientific talks and presentations; disseminate new clinical data accurately per label
• Ensure strong medical presence at investigational sites and key centers; provide scientific leadership
• Support research grants planning and management,



including non-interventional studies and PMCF
• Collaborate with internal teams and support regulatory/compliance in all activities
• Track field activities and communications through periodic reporting
• Support internal training of commercial colleagues on clinical data and medicines

Responsabilidades
• MD, MBA, PhD strongly desired; degree in Health Sciences required
• Experience as MSL/MSR or in Oncology/hematology preferred
• Fluency in English
• Clinical background in Epidemiology, Oncology, Immunology, Clinical Trials, molecular biology, translational medicine preferred
• Strong interpersonal, written and verbal communication skills with scientific and non-scientific audiences
• Experience in medical writing and submission to peer-reviewed journals
• Customer-oriented, science-based mindset; ability to work under deadlines
• Ability to work in a multi-functional team and adapt to new digital tools
• Knowledge of Regulatory Affairs, Drug Safety, Legal and compliance; regulatory savvy
• Willingness to travel; valid driver’s license
• Understanding of drug development, pharmacovigilance and regulatory legislation; Clinical Research knowledge

Requisitos principales
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📌 MSR Oncology Genitourinary tumors (Cataluña) (Gerona)
🏢 Pfizer
📍 Gerona