Medtronic's Neuromodulation and Pelvic Health team needs to generate and disseminate clinical evidence to support therapy innovation, adoption, and access, incorporating AI and real-world evidence (RWE) to transform patient outcomes.
Requirements
- 3+ years of leadership experience in a healthcare setting, ideally in medical devices or regulated clinical research
- Knowledge of neuromodulation, pain, or neuroscience therapy areas
- Experience influencing upstream pipeline and downstream reimbursement/market access strategy
Responsibilities
- Leads development and execution of clinical evidence for both local and global studies, manages clinical evidence generation over all Pain and Interventional therapies products (SCS, TDD, and Interventional).
- Evidence generated must be scientifically valid, meet all relevant reimbursement and regulatory requirements and be conducted within ethical guidelines.
- Evidence generation must be a fair assessment of the safety and effectiveness of the tested product (s), as well as patient reported outcomes, including but not limited to quality of life and satisfaction.
- Translate business and therapy strategies into clinical evidence plans to enable clinical insights which drive evidence generation
- Support product lifecycle alignment with R&D, Regulatory, HEOR, Marketing, and Clinical Affairs
- Partner with key opinion leaders and scientific advisors to generate high-quality, high-impact evidence
- Collaborate with cross-functional stakeholders to drive timely, impactful dissemination
Other
- Bachelor’s degree and 5+ years of clinical research, strategy, or program management experience
- OR advanced degree with 3+ years of clinical research, strategy, or program management experience
- Performs management duties for the Pain Therapies clinical evidence team
- Ensures team achieves committed deliverables
- Represents Medtronic from a clinical research perspective within the country / region and also collects feedback from local customers and authorities.
