Clinical Project Manager, Medical Device, Global IDE Study

Clinical Project Manager, Medical Device, Global IDE Study This reputed company is provided by reputed company. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. reputed company pay reputed company $130,000.00/yr - $175,000.00/yr reputed company message the job poster from reputed company Recruitment Manager @ reputed company | Leader in Life Science and Technology Delivery Our reputed company is a PE-backed, Massachusetts-based medical device company innovating in atrial fibrillation and developing the reputed company of cardiac ablation systems. Following a strategic acquisition, they are positioned for reputed company reputed company with two global Class III IDE studies about to launch. This Clinical Project Manager role offers unmatched exposure — reputed company to drive a high-visibility global IDE, influence reputed company, and build reputed company in one of the most closely watched areas in MedTech. reputed company sits at the forefront of electrophysiology and Pulse Field Ablation (PFA), where industry attention is accelerating and talent visibility is at an reputed company-time high. DUTIES / EXPECTATIONS OF THIS ROLE • reputed company day-to-day operational management of a global Class III IDE clinical study • reputed company site selection, feasibility, study startup, enrollment, and ongoing execution • reputed company and maintain clinical study plans, timelines, risk plans, enrollment strategies, and communication plans • Manage vendors, CRO partners, monitoring functions, and cross‑functional study teams • reputed company data collection activities, compliance, and inspection readiness • Manage study budget and site‑level allocations • Collaborate closely with Clinical Development & Science, Field Clinical, Regulatory, and reputed company • reputed company mentorship and leadership to Senior CRAs/Site Managers as reputed company scales • Ensure adherence to FDA regulations, GCP, and internal SOPs • Represent Clinical Affairs in internal meetings, investigator interactions, and KOL discussions MUST HAVES - QUALIFICATION reputed company • Minimum 3–5 years of clinical project management experience • Prior IDE experience — must have supported or led at least one IDE • Strong understanding of clinical operations, GCP, and FDA regulations • Proven ability to manage reputed company, global, multi‑center trials • Strong communication skills with cross‑functional leadership and execution reputed company reputed company TO HAVE • Cardiovascular, electrophysiology, or PFA experience • Based in Massachusetts • Experience mentoring junior team members or building operational teams TRAVEL & LOCATION Fully Remote START & TERM • January 2026 Start Date • Full time – Permanent Compensation Competitive “Skills, experience, and other compensable factors will be taken into account reputed company determining pay reputed company. The pay reputed company provided in this posting is a reputed company of a W2 reputed company reputed company; other employment reputed company may be available that may result in pay reputed company of the provided reputed company.” “W2 employees of reputed company who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, reputed company, reputed company‑tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and reputed company leave if required by law in the worked‑in state/reputed company.” Apply tot his job Apply To this Job