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BeOne Medicines

Medical Advisor, Early Pipeline – Scientific Engagement

BeOne Medicines

Medical Advisor shaping oncology evidence-generation and scientific engagement strategy for BeOne, a global company developing affordable cancer treatments. Partnering with investigators and cross-functional teams across German Medical Affairs.

Posted 8/4/2026full-time🇩🇪 GermanyMid-LevelSenior💰 €87,000 - €108,700 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Medical Affairs strategy execution, clinical trial management, and stakeholder engagement within the healthcare landscape. Proficient in analyzing scientific data, developing advocacy plans, and collaborating cross-functionally to address unmet medical needs.

Highest-signal resume keywords
Medical Affairs Strategy ExecutionClinical Trial ManagementStakeholder EngagementRegulatory Compliance KnowledgeProject Management Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial DesignData AnalysisScientific CommunicationMedical Engagement PlanningEvidence GenerationProtocol DevelopmentFeasibility AssessmentRecruitment SupportMarket Dynamics UnderstandingTherapeutic Area Knowledge
Soft Skills
Interpersonal SkillsCommunication SkillsEmotional IntelligenceCollaborationFlexibility
Tools & Technologies
Microsoft Office SuiteElectronic CRM Systems
Industry Keywords
Healthcare SystemCompliance StandardsRegulatory RequirementsKOL EngagementResearch Study ExecutionScientific CongressesAdvocacy OrganizationsClinical OperationsInvestigator-Initiated TrialsMulticulturalism

About the role

Key responsibilities & impact
  • Shape and execute country Medical Affairs strategy within the assigned therapeutic area
  • Lead the country-level scientific engagement strategy for priority investigators and external experts
  • Build strategic partnerships with KOLs, research centers, HCPs, scientific societies, and advocacy organizations
  • Develop, implement, and monitor Medical Engagement and advocacy plans
  • Support clinical study feasibility, investigator and site identification, site relationships, study start-up, recruitment, and close-out
  • Deliver evidence-based scientific information and facilitate responses to unsolicited medical information requests
  • Plan, organize, and chair local medical meetings, advisory boards, consultancy meetings, and investigator meetings
  • Support and follow up on scientific congresses and relevant events
  • Represent German Medical Affairs in regional and global governance meetings
  • Identify unmet medical needs, emerging trends, evidence gaps, and innovation opportunities
  • Capture, document, assess, synthesize, and analyze stakeholder and field-based insights
  • Lead local evidence-generation initiatives and provide medical input into clinical study design and protocol optimization
  • Oversee and facilitate Investigator-Initiated Trial proposals and communicate generated data
  • Collaborate with local, European, and global Medical Affairs, Clinical Operations, Development, Market Access, Marketing, and Sales teams
  • Communicate medical insights and provide scientific expertise, content review, medical information support, and internal team education

Requirements

What you’ll need
  • Minimum 6 years of proven experience in Medical Affairs, preferably with field-based responsibilities
  • Experience conducting company-sponsored clinical trials, including site feasibility, study start-up, investigator engagement, recruitment support, or protocol development
  • Good understanding of the relevant therapeutic area landscape and local market dynamics
  • Excellent interpersonal and communication skills
  • Strong knowledge of treatment guidelines, compliance standards, local/regional regulatory requirements, and the healthcare system
  • Ability to identify and address unmet medical, educational, and research needs
  • Advanced analytical capabilities to collect, analyze, and interpret scientific data and insights
  • Solid understanding of research study design and execution and their strategic implications
  • Ability to work collaboratively and cross-functionally
  • Strong project management skills
  • High emotional intelligence and appreciation of diversity and multiculturalism
  • Excellent medical and scientific communication skills
  • Flexibility and resilience in complex and high-pressure situations
  • Proficiency with Microsoft Office Suite and experience with electronic CRM systems
  • Fluency in verbal and written English and German
  • Any other major European language is advantageous
  • Willingness to travel extensively, up to 70% of the time
  • Valid driving license required

Benefits

Comp & perks
  • Salary range of 87,000.00 EUR - 108,700.00 EUR
  • Equal opportunity employment
  • Extensive travel and participation in congresses and medical meetings as part of the role