Clinical Project Manager Job at EPM Scientific, Trenton, NJ

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  • EPM Scientific
  • Trenton, NJ

Job Description

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.

Key Responsibilities

  • 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.

Qualifications

  • 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!

Job Tags

Full time, Local area,

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