Medical Science Liaison – Sao Paulo, South Region

BeOne Medicines

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

Posted 11/5/2026full-timeRemote • BrazilMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical oncology and medical affairs, with a strong ability to build relationships with healthcare professionals and manage strategic partnerships. Proficient in interpreting scientific data and developing compliant regional strategies to enhance patient outcomes.

Highest-signal resume keywords

Clinical Oncology ExperiencePharmaceutical/Biotech Industry ExperienceProject Management SkillsStrong Communication SkillsMD, PharmD, PhD, or DO Degree

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ExperienceResearch Study DesignData InterpretationStrategic PlanningTraining Initiative Design

Soft Skills

Interpersonal SkillsOrganizational SkillsCross-Functional CollaborationFlexibilityCreative Thinking

Tools & Technologies

Microsoft 365Veeva

Industry Keywords

HematologyOncologyMedical AffairsHealthcare Delivery SystemManaged Care

About the role

Key responsibilities & impact

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

What you’ll need

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