Medical Science Liaison – Sao Paulo, South Region

🔥 13 minutes ago

🇧🇷 Brazil – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✨ Medical Science Liaison

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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BeOne Medicines

WebsiteLinkedInAll Job Openings

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

• Support BeOne Medicines’ pre-clinical and clinical pipeline development by coordinating external collaborations and research activities with healthcare providers and academic experts • Ensure strong internal partnership across the organization and report to the Medical Affairs Director • Serve as a scientific expert and key link between BeOne Medicines and the medical community through dissemination and discussion of scientific data • Establish long-term scientific strategies and relationships with physicians, scientists, medical associations, and academic centers • Develop regional strategies supporting compliant relationships with Opinion Leaders, Research Collaborators, and Key Organizations for pipeline development in solid tumors and/or hematology • Provide pre-launch and post-launch Medical Affairs support • Collaborate with Medical Affairs, Clinical Development, Program Leadership, Clinical Operations, Legal, Compliance, New Product Planning, Safety/Pharmacovigilance, Molecular Diagnostics, Marketing, Sales, and Translational Research • Serve as an internal resource for clinical and scientific information gained through medical interactions • Provide feedback and information to internal stakeholders on emerging clinical and scientific trends • Develop territory plans that inform healthcare professionals and support improved patient outcomes • Establish and maintain peer-to-peer relationships with regional and national opinion leaders and healthcare providers • Facilitate and monitor strategic partnerships with scientific and clinical experts and serve as an enterprise-level point of contact with relevant organizations • Contribute to therapeutic-area and indication research and competitor analysis • Assist in developing and executing regional medical meetings, advisory boards, consultant meetings, and investigator meetings • Identify and verify investigators and sites for company-sponsored clinical trials • Liaise for submission and review of Investigator-Sponsored Research proposals • Support major and regional congresses and engage thought leaders • Provide balanced and accurate information to regional formulary decision makers and Pharmacy and Therapeutics committee members • Build relationships with internal experts and identify process-improvement opportunities • Develop, track, execute, and report on goals and objectives • Support Medical Affairs budget planning and management • Maintain accountability for compliant business practices

🎯 Requirements

• Fluent English (Spoken and Written is Preferred) • Preferred experience in the pharmaceutical/biotech industry • MD, PharmD, PhD, or DO in a clinical and/or scientific profession, with a minimum of 5 years of clinical experience and/or demonstrated success in biotech/pharmaceutical companies; OR NP, PA, or Master’s degree in a clinical and/or scientific profession, with a minimum of 7 years of clinical experience and/or demonstrated success in biotech/pharmaceutical companies • Clinical oncology experience in hematology/oncology; candidates with exceptional experience in other therapeutic areas may be considered if they demonstrate clear potential to apply their skills to oncology • Established relationships with relevant healthcare professionals in the region • High level of written and verbal communication, interpersonal, organizational, and cross-functional collaboration skills • Flexibility to work with colleagues in a global setting • Ability to engage in work-related travel approximately 60–70% • Strong understanding of relevant disease states, treatment decision algorithms, and the healthcare delivery system, including managed care and its impact on patient care and the pharmaceutical industry • Ability to identify unmet medical, educational, and research needs at local and regional levels • Ability to interpret key scientific data and translate findings into educational and research insights • Understanding of research study design and execution and their strategic implications • Ability to design and/or lead training initiatives and best practices • Proven ability to drive high-quality results as a strategic and creative thinker and to thrive amid ambiguity and change • Strong project management, time management, and organizational skills, with demonstrated success implementing business-critical projects • PC literacy required; proficiency in Microsoft 365 applications, including Outlook, Word, Excel, and PowerPoint, and experience with Veeva

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