Senior Oncology Medical Science Liaison — UK

Genmab; Greater London; On-site; GBP 66,000 - 99,000; Full time

Benefits offered by this job

Pension

Health & wellness

Paid time off

Employee support programs

Job summary

Genmab is seeking a Senior Medical Science Liaison based in the UK to lead non-promotional scientific exchange with healthcare professionals in oncology. Travel ~60% to cover national and international sites, collaborating with cross-functional teams to advance assets.

You will provide up-to-date clinical data, support investigator-initiated studies, and help inform publication planning while ensuring ABPI compliance and high ethical standards.

Qualifications

• Advanced Scientific or Medical Degree (Pharm D, PhD, MD) or relevant clinical background.
• Minimum 3 years of MSL/Medical Affairs experience in Oncology.
• Strong understanding of ABPI Codes of Practice and other compliance regulations.
• Excellent interpersonal communication and presentation skills.
• Fluency in English required.
• Demonstrated ability to adopt and use MS Office and multiple business applications.

Responsibilities

• Act as local expert for Genmab’s areas of interest and maintain up-to-date knowledge.
• Establish and maintain relationships with healthcare/scientific professionals.
• Provide clinical and scientific information to HCPs in response to requests.
• Deliver non-promotional scientific exchange on disease area and data.
• Gather insights to inform development and commercialization strategies.
• Represent Genmab at medical conferences and advisory boards.
• Engage with payers regarding the value of Genmab products.
• Collaborate with cross-functional teams across medical, development ops, market access and commercial.

Skills

English fluency

Communication skills

MS Office

Multi-tasking

Education

Advanced scientific/medical degree

Job description

Genmab is seeking a Senior Medical Science Liaison based in the UK to lead non-promotional scientific exchange with healthcare professionals in oncology. Travel ~60% to cover national and international sites, collaborating with cross-functional teams to advance assets.

You will provide up-to-date clinical data, support investigator-initiated studies, and help inform publication planning while ensuring ABPI compliance and high ethical standards.