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BeOne

Global oncology therapeutics discovery, development, manufacturing

Senior Medical Science Liaison - Solid Tumors

Biology & BiotechConfirmed live in the last 24 hours
Full-timeRemote in Germany€109.1k - €136.4k

About the Job

Requirements

  • MD, PhD, or PharmD with at least 4 years of experience, or a Master’s degree with at least 6 years of experience, and a proven pharmaceutical-industry track record; relevant clinical, scientific, or medical affairs experience in the therapeutic area is preferred.
  • Experience in medical affairs, ideally in Lung Cancer and/or upper-GI Cancer; experience with immune checkpoint inhibitors is a plus.
  • Excellent verbal and written communication skills and stakeholder engagement capabilities.
  • Deep understanding of the relevant therapeutic-area landscape and local market dynamics.
  • In-depth understanding of disease states, treatment decision algorithms, treatment guidelines, compliance standards, and local and regional regulatory requirements.
  • Ability to identify and address unmet medical, educational, and research needs within the medical community.
  • Ability to translate scientific and clinical data into actionable medical insights.
  • Strong project management skills and demonstrated ability to manage projects and/or colleagues in successful implementation of business-critical projects.
  • Ability to collaborate effectively in a dynamic, global environment.
  • Clinical research experience is preferred.
  • Strong time-management and organizational skills.

Responsibilities

  • Build and maintain professional relationships and partnerships with healthcare professionals, key opinion leaders, and other external stakeholders to exchange scientific and medical information about therapeutic areas, products, and pipeline.
  • Plan, develop, and execute Medical Affairs tactics and activities within the assigned geographic area; use regular field interactions to collect, analyze, and communicate actionable medical insights, emerging trends, and unmet medical needs to internal stakeholders.
  • Collaborate with Medical Affairs, Clinical Operations, and other internal teams while maintaining medical independence and complying with regulatory, ethical, and company standards.
  • Deliver accurate, high-quality, non-promotional scientific exchange with healthcare professionals and key opinion leaders.
  • Develop and execute tactics to communicate complex scientific information to the healthcare community in coordination with the Therapeutic Area Lead.
  • Provide accurate, current scientific communication about pipeline products and indications in development at healthcare professionals’ request.
  • Facilitate responses to unsolicited medical-information requests, often in direct collaboration with Medical Information Services personnel.
  • Provide first-line scientific communication about assigned products and the environment in response to healthcare professionals’ requests; present product clinical and development data and publications, including data outside marketing authorization when unsolicited, through field engagements or scientific meetings.
  • Support, attend, and follow up on local, national, regional, and international scientific congresses and events.
  • Support enterprise activities including booth duty, session coverage, and insight gathering; participate in planning and executing omnichannel initiatives.
  • Identify and map medical experts and national or regional institutional networks, and develop and maintain engagement plans in the assigned therapeutic area and location.
  • Establish, develop, and maintain long-term professional relationships with healthcare professionals and cooperative groups in the company’s therapeutic areas.
  • Propose, initiate, implement, and monitor scientific partnerships aligned with cross-functional strategy for key clinical sites and hospitals in the assigned region.
  • Participate in planning, organizing, and executing medical events such as congresses and advisory boards.
  • Identify and support the identification and verification of investigators and clinical sites for company-sponsored clinical trials.
  • Monitor developments in the therapeutic-area landscape and standards of care.
  • Collaborate with Clinical Operations on site feasibility assessments, planning and onboarding of clinical-trial sites, and ongoing site and trial follow-up in the assigned region.
  • Serve as the primary territory liaison for receiving, preliminarily reviewing, and submitting Investigator Sponsored Research proposals, facilitating the process from concept submission through publication.
  • Collect, analyze, and communicate field-based medical insights to internal stakeholders.
  • Provide scientific input and field-based feedback to define, update, and support Medical Affairs strategies.
  • Identify unmet medical needs and emerging trends in the therapeutic area.
  • Plan, organize, and chair clinically relevant local medical meetings, including advisory boards, consultancy meetings, and local investigator meetings, in collaboration with the Therapeutic Area Lead.
  • Build relationships with the Medical Affairs Department and collaborate with European and Global Medical Affairs teams.
  • Provide scientific and medical expertise to cross-functional teams.
  • Interact with sales teams on cross-functional projects unrelated to products.
  • Organize local scientific events, review scientific literature, and support the Medical Manager where applicable, or lead development and delivery of scientific training programs and medical updates to the Field Sales Force.
  • Work with internal stakeholders to develop and execute a medical plan designed to meet shared objectives.

Desired Qualifications

  • Previous experience in Lung Cancer and/or upper-GI Cancer is preferred; experience with immune checkpoint inhibitors is a plus.
  • Clinical research experience is preferred.

About the Company

BeOne

Global oncology therapeutics discovery, development, manufacturing

BeOne Medicines discovers, develops, and commercializes oncology therapies worldwide, focusing on hematologic cancers and solid tumors. Its products work by leveraging internal R&D and clinical development to bring therapies to market quickly, with Brukinsa serving as a leading backbone in the US and European markets. It differentiates itself through a large-scale global clinical network and cost-efficient development and manufacturing that support high margins and a focus on large-market cancer indications. Its goal is to expand access to high-impact, affordable cancer treatments across more than 45 countries while growing its pipeline into immunology and solid tumors.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Dongcheng District, China
Founded
2010

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