Medical Science Liaison

About the role

BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 10,000 colleagues spans five continents, with administrative offices in Basel, Beijing, and Cambridge, U.S. To learn more about BeOne , please visit www.beonemedicines.com and follow us on LinkedIn and X (formerly known as Twitter). 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. Job Description: The Medical Science Liaison will establish and maintain relationships with key healthcare professionals (HCPs) to create a better understanding of the BeOne Medicines's products and increase product awareness. MSL will be responsible for in-field(mainly, but not limited) execution of the medical affairs strategy of the designated therapeutic area and provide scientific support for marketed products and products in development. Main Responsibilities This position supports the execution of the Medical Affairs plan in the field (mainly, but not limited) for the designated therapeutic area. The Medical Science Liaison is the vital contact with Key Opinion Leaders (KOL), Health Care Providers (HCP) and other key stakeholders for BeOne Medicines. The Medical Science Liaison will identify scientific opportunities to partner with external stakeholders and generate insights to enhance BeOne Medicines's Medical Affairs (MA) and clinical development plans. The Medical Science Liaison is required to combine their clinical expertise with strong business acumen and presentation skills to serve as the key channel of information for KOLs via scientific exchange. Additional representative responsibilities include, but are not necessarily limited to, the following: Execute the Field Engagement Plan and support business objectives, such as Advisory board meetings, national/regional educational meetings, scientific conferences, KOL development programs, etc., and ensure its successful implementation. Implement scientific communication strategy including key publications from BeOne Medicines trials and key messages in therapeutic area and BeOne Medicines brands to support business strategies and life cycle management. Assist with execution of the MA plan to develop integrated KOL list, ensure sufficient KOL coverage by field visits & educational meetings, scientific projects, speaker training, etc. and ensure proper tracking of these activities. Work with KOLs in the relevant field to understand current clinical practice, challenges, and areas of unmet need. Share insights with the wider organization to inform and guide strategy as needed. Actively participate in cross functional meetings and share external customers' insights with internal stakeholders. Work closely with BeOne Medicines cross functional team members to establish and maintain strong relationships with key opinion leaders for and on behalf of BeOne Medicines in all relevant areas to promote the Company's reputation, dedication to patients, and expertise in these areas. Serve as a liaison for the submission and review of Investigator Initiated Trial (IIT) proposals Support in HCP related requests / program for pre-approved products, namely NPP (Named Patient Program), EAP (Early Access Program) Liase with the Local Safety Officer for the following accountabilities (not limited to): Support local RMP activities with medical advisor Support the Global Clinical Operations team in assessing trials, identifying trial sites & new investigators, managing trials, and ensuring timely delivery of our clinical trial program in Korea. Ensure compliance with country directives and ensure all MA activities are conducted with the utmost integrity. Qualification Required: Education Required: Pharmacist, R.N or equivalent with significant experience in all aspects of clinical trials and professional knowledge and skills working with oncology therapeutics. Experience in Solid Tumor indications (e.g. Lung, Gastric, Liver, Esophagus) or Hematology indications (e.g. Lymphoma, Myeloma) is preferred Experience/ Qualifications: Relevant pharmaceutical or related industry experience (4~8 years or longer) in hemato-oncology with a proven track record of contribution to commercial, medical and/or clinical development strategies Solid peer relationships with and exposure to external scientific and clinical experts and Key Opinion Leaders; demonstrated ability

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