Associate Director, Medical Science Liaison, Oncology - West
Immunocore
July 02, 2026
On-site
United States
Medical Affairs
Location: Remote US (West Territory: California, Arizona, Nevada, Hawaii)
Key Responsibilities:
- Serve as primary field-based point of contact with healthcare providers (HCPs), including clinical investigators.
- Deliver and facilitate medical education and communications, research, and scientific insight gathering.
- Maintain advanced knowledge of immuno-oncology, relevant disease areas, and Immunocore/competitor products and therapeutic options.
- Collaborate cross-functionally to align activities with Immunocore strategy and support best patient care.
- Maintain and develop relationships with KOLs to expand research, advisory, and educational partnerships.
- Ensure work is conducted to the highest ethical compliance, ethics, and safety standards and in accordance with local laws/regulations.
- Act as an educational resource to internal stakeholders; provide external scientific expertise at HCP meetings, conferences, advisory boards, investigator meetings, and patient advocacy groups.
- Respond to unsolicited requests for medical information in a balanced, objective manner.
- Lead congress symposiums and other educational programs; provide tailored clinical presentations; support early access programs.
- Identify/map HCPs and networks; disseminate key field insights with cross-functional partners.
- Support congress planning/implementation and help resolve HCP needs/issues.
- Support trial site identification; facilitate investigator communication; lead ESR proposal collation, review, and maintenance of approved studies.
Experience & Qualifications:
- 3–5+ years MSL experience.
- Advanced degree: MD, PhD, or PharmD.
- 3+ years oncology experience (preferably immuno-oncology and melanoma) required.
- Knowledge of clinical research design and GCP in oncology/immune oncology.
- Understanding of clinical trial design and study analysis, including HEOR/cost effectiveness.
- Knowledge of local healthcare systems and treatment guidelines.
- Ability to build trust with KOLs/investigators/HCPs.
- Knowledge of relevant laws/regulations.
- Excellent presentation and communication skills.
- Ability to tailor complex scientific information to varied audiences.
Travel: ~60%
Benefits/Compensation:
- $170,000–$225,000; standard company benefits (medical, dental, vision, time off, 401k) and eligibility for annual incentive plans.
Key Responsibilities:
- Serve as primary field-based point of contact with healthcare providers (HCPs), including clinical investigators.
- Deliver and facilitate medical education and communications, research, and scientific insight gathering.
- Maintain advanced knowledge of immuno-oncology, relevant disease areas, and Immunocore/competitor products and therapeutic options.
- Collaborate cross-functionally to align activities with Immunocore strategy and support best patient care.
- Maintain and develop relationships with KOLs to expand research, advisory, and educational partnerships.
- Ensure work is conducted to the highest ethical compliance, ethics, and safety standards and in accordance with local laws/regulations.
- Act as an educational resource to internal stakeholders; provide external scientific expertise at HCP meetings, conferences, advisory boards, investigator meetings, and patient advocacy groups.
- Respond to unsolicited requests for medical information in a balanced, objective manner.
- Lead congress symposiums and other educational programs; provide tailored clinical presentations; support early access programs.
- Identify/map HCPs and networks; disseminate key field insights with cross-functional partners.
- Support congress planning/implementation and help resolve HCP needs/issues.
- Support trial site identification; facilitate investigator communication; lead ESR proposal collation, review, and maintenance of approved studies.
Experience & Qualifications:
- 3–5+ years MSL experience.
- Advanced degree: MD, PhD, or PharmD.
- 3+ years oncology experience (preferably immuno-oncology and melanoma) required.
- Knowledge of clinical research design and GCP in oncology/immune oncology.
- Understanding of clinical trial design and study analysis, including HEOR/cost effectiveness.
- Knowledge of local healthcare systems and treatment guidelines.
- Ability to build trust with KOLs/investigators/HCPs.
- Knowledge of relevant laws/regulations.
- Excellent presentation and communication skills.
- Ability to tailor complex scientific information to varied audiences.
Travel: ~60%
Benefits/Compensation:
- $170,000–$225,000; standard company benefits (medical, dental, vision, time off, 401k) and eligibility for annual incentive plans.