Clinical Project Manager, Medical Device, Global IDE Study

Clinical Project Manager, Medical Device, Global IDE Study This range is provided by Eliassen Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $130,000.00/yr - $175,000.00/yr Direct message the job poster from Eliassen Group Recruitment Manager @ Eliassen Group | Leader in Life Science and Technology Delivery Our client is a PE-backed, Massachusetts-based medical device company innovating in atrial fibrillation and developing the next generation of cardiac ablation systems. Following a strategic acquisition, they are positioned for rapid growth with two global Class III IDE studies about to launch. This Clinical Project Manager role offers unmatched exposure — the opportunity to drive a high-visibility global IDE, influence strategy, and build a team in one of the most closely watched areas in MedTech. The company sits at the forefront of electrophysiology and Pulse Field Ablation (PFA), where industry attention is accelerating and talent visibility is at an all-time high. DUTIES / EXPECTATIONS OF THIS ROLE • Lead day-to-day operational management of a global Class III IDE clinical study • Oversee site selection, feasibility, study startup, enrollment, and ongoing execution • Develop and maintain clinical study plans, timelines, risk plans, enrollment strategies, and communication plans • Manage vendors, CRO partners, monitoring functions, and cross‑functional study teams • Oversee data collection activities, compliance, and inspection readiness • Manage study budget and site‑level allocations • Collaborate closely with Clinical Development & Science, Field Clinical, Regulatory, and Quality • Provide mentorship and leadership to Senior CRAs/Site Managers as the team scales • Ensure adherence to FDA regulations, GCP, and internal SOPs • Represent Clinical Affairs in internal meetings, investigator interactions, and KOL discussions MUST HAVES - QUALIFICATION SUMMARY • 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 complex, global, multi‑center trials • Strong communication skills with cross‑functional leadership and execution focus NICE 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 when determining pay rate. The pay range provided in this posting is a reflection of a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.” “W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre‑tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick leave if required by law in the worked‑in state/locality.” Apply tot his job