Clinical Medical Advisor

The Company

Our client is a global biotechnology company focused on developing innovative antibody-based therapies to treat cancer and other serious diseases. With a strong international presence, they collaborate with leading pharmaceutical partners and are known for advancing cutting‑edge science to improve patient outcomes.

The Medical Advisor supports clinical trials by providing medical and scientific expertise to study teams and stakeholders across the North Europe cluster. The role focuses on ensuring patient safety, scientific integrity, and operational feasibility throughout the clinical trial process. Responsibilities include advising on study protocols, feasibility assessments, stakeholder collaboration, and engaging with investigators and Key Opinion Leaders.

• Provide medical and scientific expertise to clinical trial teams to ensure patient safety and scientific integrity throughout the study lifecycle.
• Support study design, protocol development, feasibility assessments, patient recruitment strategies, and site selection activities.
• Act as the primary medical contact for investigators, clinical sites, and internal stakeholders including CSU, R&D, and Medical Affairs teams.
• Build and maintain strong relationships with Key Opinion Leaders (KOLs) to facilitate scientific exchange, gather study insights, and support trial success.
• Deliver medical training and guidance to study teams while effectively bridging global and local clinical perspectives in a complex stakeholder environment.

• MD degree preferred, or PhD/Pharm
  
  D in Life Sciences, with strong medical and scientific expertise in clinical research or drug development.
• Proven experience in clinical practice, clinical trials, pharmaceutical research, or clinical development within a regulated healthcare environment.
• Solid understanding of ICH-GCP guidelines, clinical trial regulations, patient safety standards, and study protocol processes.
• Strong stakeholder management and communication skills with experience collaborating with investigators, KOLs, Medical Affairs, R&D, and cross‑functional teams.
• Ability to work independently in a fast‑paced environment, demonstrating proactivity, adaptability, problem‑solving skills, and fluency in English.