Senior Medical Science Liaison, Solid Tumors - South Germany

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

The Senior Medical Science Liaison (MSL) is the field-based Medical Affairs’ representative in relation to the external medical community. This role is responsible for building and maintaining professional relationships and partnerships with Healthcare Professionals (HCPs), Key Opinion Leaders (KOLs) and other external stakeholders to exchange scientific and medical information related to BeOne’s therapeutic areas, products and pipeline. The Senior MSL combines in-depth scientific expertise with strong external engagement to plan, develop and execute Medical Affairs tactics and activities within the assigned geographic area, and, through regular field interactions, collects, analyzes and communicates actionable medical insights, emerging trends and unmet medical needs to internal stakeholders, contributing to the definition and execution of medical affairs strategies.

The role collaborates closely within Medical Affairs, Clinical Operations, and other internal teams, while maintaining medical independence and ensuring full compliance with regulatory, ethical, and company standards. MSLs contribute to advancing scientific knowledge, supporting the safe and appropriate use of BeOne products, and strengthening the company’s scientific credibility within the healthcare community.

South Germany area comprises Bavaria and parts of Baden-Würtemberg.

• Deliver high-quality, accurate and non-promotional scientific exchange with healthcare professionals (HCPs) and Key Opinion Leaders (KOLs).
• Develop and execute tactics for communicating complex scientific information to the healthcare community, in communication with the TAL.
• Provide accurate and up-to-date scientific communication on BeOne’s pipeline products and/or indications in development, at the request of Healthcare Professionals.
• Facilitate responses to unsolicited requests for medical information, often in direct collaboration with BeOne Medical Information Services personnel as appropriate.
• Provide first-line scientific communication on the assigned products/environment in response to requests from HCPs.
• Present data on BeOne products, including clinical data, development data, publications and, upon unsolicited requests, data outside the scope of marketing authorization, through ad-hoc field engagements or during scientific meetings.
• Support, attend, and follow up on local, national, regional and international scientific congresses and events.
• Support enterprise activities such as booth duty, session coverage, and insight gathering, as well as partaking in the planning and execution of omnichannel initiatives, thereby taking a shared responsibility for achieving our enterprise goals.

• Identify, map, develop and maintain engagement plans for medical experts and national or regional institutional networks (healthcare decision-makers, public health organizations, etc.) in the assigned therapeutic area and location.
• Establish, develop and maintain long-term professional relationships with HCPs and cooperative groups in BeOne's therapeutic areas.
• Propose, initiate, implement and monitor scientific partnerships in line with the cross-functional strategy established for the key clinical sites and hospitals in the assigned region.
• Participate in the planning, organization and execution of medical events (e.g. congresses and advisory boards) according to needs.

• Identify and support the identification and verification of investigators and clinical sites for company-sponsored clinical trials.
• Contribute to or conduct monitoring on developments in the therapeutic area landscape and standards of care.
• In collaboration with clinical operations, participate in site feasibility assessments, planning and onboarding of clinical trials…