About the Role
Leads the development and execution of clinical affairs strategy to support product lifecycle management, regulatory submissions, and market access initiatives.
Responsibilities
- Direct the creation and implementation of clinical development plans for assigned products
- Oversee the design and execution of clinical trials and real-world evidence studies
- Collaborate with cross-functional teams to align clinical data with regulatory requirements
- Ensure clinical strategies support global product approvals and market differentiation
- Manage clinical budgets and resource allocation for maximum efficiency
- Lead external partners, including CROs and clinical sites, to ensure study compliance
- Evaluate emerging clinical data to inform product positioning and lifecycle planning
- Serve as primary clinical liaison to regulatory authorities during submission phases
- Maintain oversight of clinical data collection, analysis, and reporting timelines
- Ensure adherence to ethical standards, GCP, and applicable regulatory guidelines
- Develop integrated evidence generation plans across product portfolios
- Provide clinical input into product labeling and promotional materials
- Support health technology assessments and payer engagement with clinical data
- Monitor competitive landscape to identify gaps and opportunities in clinical evidence
- Lead clinical training for internal stakeholders and field teams
- Drive continuous improvement in clinical operations and study methodologies
- Coordinate with quality and compliance teams to address audit findings
- Prepare and present clinical findings to senior management and governance boards
- Manage risk mitigation strategies for clinical development programs
- Support post-market clinical follow-up as required by global regulations
Compensation
Competitive salary and benefits package offered
Work Arrangement
Hybrid work model with flexibility based on role and location
Team
Part of the global clinical team within a medical technology organization
Why This Role Matters
This position plays a critical role in shaping the clinical evidence that supports product approvals, safety, and market success across diverse therapeutic areas.
Growth Opportunities
Opportunities exist for strategic influence on product development and advancement into broader leadership roles within clinical and medical affairs.
May be available based on business needs and eligibility
