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Senior Medical Science Liaison, Solid Tumors

🔥 0 minutes ago

🇩🇪 Germany – Remote

💵 €109.1k - €136.4k / year

⏰ Full Time

🟠 Senior

✨ Medical Science Liaison

Where this job comes from

Posted on BeOne Medicines's careers page, not through a job board

First seen by Remote Rocketship 0 minutes ago

Logo of BeOne Medicines

BeOne Medicines

10,000+ employees

Founded 2010

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

Biotechnology • Healthcare • Pharmaceuticals

BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.

📋 Description

• Serve as the field-based Medical Affairs representative to the external medical community • Build and maintain professional relationships with HCPs, KOLs, cooperative groups, healthcare decision-makers and other external stakeholders • Exchange scientific and medical information related to BeOne’s therapeutic areas, products and pipeline • Plan, develop and execute Medical Affairs tactics and activities within the assigned geographic area • Collect, analyze and communicate actionable medical insights, emerging trends and unmet medical needs to internal stakeholders • Deliver accurate, non-promotional scientific exchange and communicate complex scientific information • Provide scientific communication on pipeline products, indications in development, clinical data, development data and publications • Facilitate responses to unsolicited medical information requests • Support, attend and follow up on scientific congresses and events • Support booth duty, session coverage, insight gathering and omnichannel initiatives • Identify and maintain engagement plans for medical experts and institutional networks • Establish and maintain long-term relationships with HCPs and cooperative groups • Propose, initiate, implement and monitor scientific partnerships with clinical sites and hospitals • Plan, organize and execute medical events including congresses and advisory boards • Identify and support investigators and clinical sites for company-sponsored clinical trials • Participate in site feasibility assessments, clinical trial site planning, onboarding and follow-up • Serve as territory liaison for Investigator Sponsored Research proposals from submission through publication • Provide scientific input and field-based feedback for Medical Affairs strategies • Plan, organize and chair local medical meetings • Collaborate with Medical Affairs, Clinical Operations, European and Global Medical Affairs and cross-functional teams • Provide scientific and medical expertise to cross-functional projects • Organize local scientific events, review scientific literature and support or lead scientific training and medical updates for the Field Sales Force • Develop and execute a medical plan with internal stakeholders

🎯 Requirements

• MD, PhD or PharmD with a minimum of 4 years’ experience, or Master’s degree with a minimum of 6 years’ experience • Proven track record in the Pharmaceutical Industry, ideally with relevant clinical, scientific and/or medical affairs experience in the relevant therapeutic area • Experience in medical affairs with previous positions in Lung Cancer and/or upper-GI Cancer • Previous work with Immunecheckpoint inhibitors considered a plus • Excellent verbal and written communication skills with strong stakeholder engagement capabilities • Deep understanding of the relevant therapeutic area landscape and local market dynamics • In-depth understanding of disease states, differential algorithms for treatment decisions, treatment guidelines, compliance standards, and local/regional regulatory requirements • Ability to identify and address unmet medical, educational and research needs within the medical community • Proven ability to translate scientific and clinical data into actionable medical insights • Clinical research experience preferred • Strong project management skills with demonstrated ability to manage projects and/or colleagues in successful implementation of business-critical projects • Ability to effectively collaborate in a dynamic and global environment • High degree of emotional intelligence and appreciation of diversity and multiculturalism • Proven ability to drive results at a high level of quality as a strategic and creative thinker • Ability to deal with ambiguity and thrive in an ever-changing environment • Strong time management and organizational skills

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