Clinical Medical Manager needed at Novo Nordisk

Your new role

• As a Clinical Medical Manager (CMM), you will be responsible for delivering industry-leading clinical trial execution excellence, securing early medical input into product development, and establishing strong scientific partnerships within current and emerging therapy areas.

Your main responsibilities will be to:

• Deliver clinical trial excellence. Partner with Therapy Area Leads and Trial Managers to ensure high-quality scientific and medical oversight.
• Gather and translate actionable clinical insights. Lead national investigator selection and engagement. Act as the local scientific expert throughout feasibility and trial execution.
• Strengthen early product development and provide early clinical and scientific input into study protocol development. Identify potential challenges early and proactively drive solutions.
• Build presence in therapy areas and communicate Novo Nordisk’s scientific narrative. Establish and maintain strong relationships with KOLs, investigators, and research institutions.
• Enable organizational readiness and deliver scientific training for Clinical Operations teams. Act as a bridge to Medical Affairs by sharing insights and facilitating early relationships.

Your new department

• You will join the Clinical Medical Management (CMM) team, a highly skilled and strategically important function within our clinical organisation. The team serves as the scientific and medical backbone supporting early clinical development, trial execution, and therapy area expansion.
• We operate at the intersection of Clinical Operations, Medical & Scientific Affairs, Global Development, and Commercial, ensuring scientific excellence and cross-functional alignment throughout the entire clinical value chain.

Your skills & qualifications
To be successful in this role you need to have:

• MD, PhD,  MPharm or equivalent.
• minimum of 2, 3+ years of experience in clinical development or medical affairs.
• Strong knowledge of ICH-GCP and clinical trial methodology.
• Excellent communication and stakeholder-management skills.
• Strong analytical mindset.
• Experience collaborating with investigators and scientific associations.

Deadline:5th Janaury,2026