
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.
🔥 12 minutes ago
⛰️ Colorado – Remote
💵 $215.4k - $275.4k / year
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
👻 Ghost score 1%
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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.
• Support BeOne Medicines’ pre-clinical and clinical pipeline development • Coordinate external collaborations and research with healthcare providers and academicians • Ensure internal partnership across the organization • Develop regional strategies supporting compliant relationships with opinion leaders, research collaborators, and key organizations • Provide pre-launch and post-launch Medical Affairs support for solid-tumor pipeline assets focused on breast and lung cancers • Collaborate with Medical Affairs, clinical development, program leadership, clinical operations, legal, compliance, new product planning, safety/pharmacovigilance, molecular diagnostics, marketing, sales, and translational research • Develop territory plans with cross-functional teams to inform HCPs and improve patient outcomes • Establish and maintain scientifically credible peer-to-peer relationships with opinion leaders and healthcare providers • Facilitate and monitor strategic partnerships with scientific and clinical experts • Serve as an enterprise-level contact for guideline-development groups, cooperative groups, and other organizations • Support major and regional congresses by engaging thought leaders • Provide balanced, accurate information to formulary decision-makers and P&T committee members when requested • Identify and vet investigators and nominate sites for company-sponsored clinical trials • Liaise on investigator-sponsored research proposal submission and review • Develop and execute regional medical meetings, including advisory boards and investigator meetings • Serve as an internal resource for clinical and scientific information • Provide internal stakeholders with feedback on emerging clinical and scientific trends • Conduct therapeutic-area research and competitor analysis • Build relationships with internal experts • Identify process-improvement opportunities • Develop, track, execute, and report goals and objectives • Support Medical Affairs budget planning and management • Maintain compliant business practices
• Clinical oncology experience in solid tumors; exceptional, transferrable experience in other therapeutic areas may be considered • Relationships with relevant HCPs in region • High level of written and verbal communication, interpersonal, organizational, and cross-functional collaboration skills • Flexibility to work with colleagues in a global setting • Able to engage in work-related travel approximately 60–70% • MD, PharmD, PhD, or DO within a clinical and/or scientific profession, with a minimum of 5 years’ clinical experience and/or success within other biotech/pharmaceutical companies; OR NP, PA, or Master’s Degree within a clinical and/or scientific profession, with a minimum of 6 years’ clinical experience and/or success within other biotech/pharmaceutical companies • Strong disease-state comprehension and differential algorithm knowledge for treatment decisions • Experience in relevant disease states • Expert understanding of healthcare delivery systems, managed care, regional medical care, and the pharmaceutical industry • Ability to identify unmet medical, educational, and research needs • Ability to interpret scientific data and translate findings into educational and research needs • Understanding of research study design, execution, and strategic implications • Ability to design and/or lead training initiatives and best practices • Proven ability to drive high-quality results • Ability to deal with ambiguity and thrive in an ever-changing environment • Effective project management and leadership skills • Strong time-management and organizational skills
• Annual bonus plan eligibility for non-commercial roles • Discretionary equity awards • Employee Stock Purchase Plan • Medical insurance • Dental insurance • Vision insurance • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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