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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading clinical development strategies for cardiovascular and metabolic disease programs, with a strong focus on regulatory compliance and strategic partnerships. Proven ability to manage complex clinical trials and mentor team members in a cross-functional environment.
Highest-signal resume keywords
Medical Degree (MD) or Advanced Degree (PhD)In Vitro Diagnostics (IVD) Study ManagementProtocol Design and Report WritingGlobal Regulatory Standards (ICH-GCP, IVDD/IVDR, MDR, FDA, NMPA)Leadership in Cross-Functional Teams
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Development StrategyClinical Utility DefinitionRegulatory FilingsClinical Document ReviewMeeting Package AuthoringClinical Process OptimizationIntellectual Property Strategy DevelopmentStudy ManagementProtocol DesignReport Writing
Soft Skills
Coaching and MentoringRelationship BuildingEffective CommunicationCultural CompetenceStrategic Thinking
Industry Keywords
CardiologyMetabolic DiseasesObesityClinical TrialsMedical DevicesDiagnosticsKey Opinion Leaders (KOLs)Medical CongressesAdvisory BoardsCompetitive Differentiation
About the role
Key responsibilities & impact- Lead the clinical development strategy for large-scale studies and complex cardiovascular and metabolic disease programs
- Define clinical utility, intended use, and claim extensions across the portfolio
- Work with Global Regulatory Affairs on global regulatory filings
- Author critical sections of meeting packages and review clinical documents for international regulatory submissions
- Act as medical lead in interactions with health authorities
- Build strategic relationships with international Key Opinion Leaders (KOLs)
- Drive development partnerships across industry and academia
- Oversee communication strategies for clinical studies
- Represent the organisation at medical congresses, advisory boards, and in key publications
- Drive competitive differentiation, innovation, and early pipeline activities
- Develop intellectual property strategies and optimise clinical processes
- Coach team members and help colleagues develop their skills and expertise
Requirements
What you’ll need- Medical degree (MD) or an advanced degree (PhD) in cardiology, metabolic diseases, obesity or related fields
- Established experience within academia, diagnostics, or the pharmaceutical industry, in the CVMD area
- Proven track record in In Vitro Diagnostics (IVD) or Medical Device study management across all stages of global clinical trials
- Experience with protocol design and report writing
- Demonstrated experience leading large, complex development programs and guiding cross-functional, matrixed teams
- Deep understanding of applicable global standards and regulations, such as ICH-GCP, IVDD/IVDR, MDR, FDA, and NMPA
- Ability to partner effectively across diverse regions, cultures, and time zones
- CV in English
Benefits
Comp & perks- Family friendly career paths
- Sustainability-focused workplace
- Healthy lifestyle support
- Flexibility of a modern workplace
- Culture of learning and sharing
- Open and candid feedback
- Opportunities to develop and grow professionally and personally
- Equal and inclusive working environment