Director, Clinical Research - Peripheral Nerve Stimulation

Medtronic; Northern (KY); Hybrid; USD 213.000 - 319.000; Vollzeit

Benefits dieser Stelle

Health, Dental and Vision Insurance

401(k) with employer match

Tuition assistance/reimbursement

Employee Stock Purchase Plan

Zusammenfassung

Medtronic is seeking a Director of Clinical Research for Neuromodulation Peripheral Nerve Stimulation. Based in Cleveland, OH or Minneapolis, MN, the role drives global clinical evidence programs across the product lifecycle, partnering with R&D, Regulatory, Medical Affairs, and Commercial teams to advance regulatory approvals and market access.

Lead studies, publish results, and guide investigators and partners to meet stringent scientific and ethical standards while ensuring alignment with

Qualifikationen

• 10+ years in clinical research or related field with leadership responsibilities.
• Experience shaping global clinical evidence strategies for regulatory, reimbursement, and commercial goals.
• Knowledge of GCP, regulatory standards, and global study requirements.

Aufgaben

• Lead the global clinical evidence strategy for Peripheral Nerve Stimulation therapies.
• Define evidence requirements addressing customer, regulatory, payer needs.
• Direct design, execution and oversight of pre-market and post-market studies.
• Ensure programs meet scientific, ethical, quality, and regulatory standards.
• Partner with cross-functional teams to align evidence with business objectives.
• Drive publication and dissemination through journals and conferences.

Kenntnisse

Clinical research leadership

Global program management

Regulatory knowledge

GCP knowledge

Cross-functional leadership

Strategic thinking

Communication

Medical affairs

Ausbildung

Bachelor's degree

Master's degree

PhD

PharmD

Jobbeschreibung

Medtronic is seeking a Director of Clinical Research for Neuromodulation Peripheral Nerve Stimulation. Based in Cleveland, OH or Minneapolis, MN, the role drives global clinical evidence programs across the product lifecycle, partnering with R&D, Regulatory, Medical Affairs, and Commercial teams to advance regulatory approvals and market access.

Lead studies, publish results, and guide investigators and partners to meet stringent scientific and ethical standards while ensuring alignment with