Clinical Project Manager
Trenton, Mercer County, New Jersey, 08628, USA
Listed on 2026-01-19
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Management
Healthcare Management, Data Science Manager -
Healthcare
Healthcare Management
Base Salary: $150K USD + Bonus | Full-Time | Remote
Globally recognized, publicly traded full-service CRO that's redefining clinical research across continents. With a footprint in over 30 countries and a workforce of 10,000+, this organization partners with thousands of biopharma and medtech innovators to bring cutting-edge therapies to market. From oncology to rare diseases, their pipeline is as diverse as their team. Leveraging AI-powered platforms and real-world data, they're not just conducting trials—they're shaping the future of medicine.
If you're a Clinical Project Manager looking to lead global studies in a collaborative, tech-forward environment, this is your chance to thrive.
- Lead and manage global Phase I-IV clinical trials across cardiovascular and oncology indications
- Oversee cross-functional teams including biometrics, regulatory affairs, medical writing, and pharmacovigilance to ensure seamless trial execution.
- Develop and maintain project timelines, budgets, and risk mitigation strategies.
- Serve as the primary point of contact for sponsors, vendors, and internal stakeholders.
- Ensure compliance with ICH-GCP, FDA, EMA, and local regulatory requirements.
- Utilize AI-enabled tools and platforms to optimize trial design and operational efficiency.
- Contribute to business operations including budgeting, forecasting, and resource planning.
- Mentor junior team members and foster a culture of excellence and innovation.
- Minimum 10 years of experience in clinical research, with at least 6 years as a Clinical Project Manager.
- Must have direct experience managing both cardiovascular and oncology studies.
- Experience across multiple phases, preferably Phase II-III.
- Global trial management experience is essential.
- CRO experience strongly preferred.
- Strong understanding of drug development processes and clinical trial regulations.
- Valid and current GCP certification required.
- Solid knowledge of local regulatory requirements in the U.S. and/or EU.
- Proven experience in budgeting and business operations related to clinical project management.
- Excellent communication, leadership, and problem-solving skills.
If you or someone you know fits this experience and shows interest, we'd love to speak with you!
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