Medical Science Liaison – Sao Paulo, South Region

This is a fully remote position, open to applicants in Brazil.

📋 Description

• Support the development of BeOne Medicines’ pre-clinical and clinical pipeline by coordinating external collaborations and research activities with healthcare providers and academic experts.

• Foster strong internal partnerships across the organization and report to the Medical Affairs Director.

• Act as a scientific expert and key liaison between BeOne Medicines and the medical community through the dissemination and discussion of scientific data.

• Develop long-term scientific strategies and relationships with physicians, scientists, medical associations, and academic institutions.

• Create regional strategies that facilitate compliant relationships with Opinion Leaders, Research Collaborators, and Key Organizations for pipeline development in solid tumors and/or hematology.

• Provide Medical Affairs support before and after product launches.

• Collaborate with various departments including 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 acquired through medical interactions.

• Supply feedback and insights to internal stakeholders regarding emerging clinical and scientific trends.

• Develop territory plans aimed at informing healthcare professionals and enhancing patient outcomes.

• Establish and nurture peer-to-peer relationships with regional and national opinion leaders and healthcare providers.

• Facilitate and oversee strategic partnerships with scientific and clinical experts and act as an enterprise-level point of contact with relevant organizations.

• Contribute to research in therapeutic areas and indications, as well as competitor analysis.

• Assist in the planning and execution of regional medical meetings, advisory boards, consultant meetings, and investigator meetings.

• Identify and validate investigators and sites for company-sponsored clinical trials.

• Act as a liaison for the submission and review of Investigator-Sponsored Research proposals.

• Support major and regional congresses while engaging with 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 opportunities for process improvement.

• Develop, track, execute, and report on goals and objectives.

• Assist in Medical Affairs budget planning and management.

• Maintain accountability for compliant business practices.

⛳️ Requirements

• Fluent in English (both spoken and written is preferred).

• Preferred experience in the pharmaceutical or biotech industry.

• MD, PharmD, PhD, or DO in a clinical and/or scientific field, with at least 5 years of clinical experience and/or demonstrated success in biotech or pharmaceutical companies; OR NP, PA, or Master’s degree in a clinical and/or scientific field, with a minimum of 7 years of clinical experience and/or demonstrated success in biotech or pharmaceutical companies.

• Clinical oncology experience in hematology/oncology; candidates with exceptional experience in other therapeutic areas may be considered if they can demonstrate clear potential for application in oncology.

• Established relationships with relevant healthcare professionals in the region.

• High proficiency in written and verbal communication, interpersonal skills, organizational abilities, and cross-functional collaboration.

• Flexibility to collaborate with colleagues in a global context.

• Willingness to travel for work approximately 60–70% of the time.

• 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.

• Capability to identify unmet medical, educational, and research needs at the local and regional levels.

• Skill in interpreting key scientific data and translating findings into educational and research insights.

• Knowledge 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 flourish amid ambiguity and change.

• Strong project management, time management, and organizational skills, with a successful track record of implementing business-critical projects.

• PC literacy required; proficiency in Microsoft 365 applications, including Outlook, Word, Excel, and PowerPoint, and experience with Veeva.

🏝️ Benefits

• Comprehensive health insurance plans.

• Opportunities for professional development and career advancement.

• Flexible working hours and remote work options.

• Employee wellness programs and initiatives.

• Competitive salary and performance-based bonuses.