Responsibilities of the Senior Clinical Project Manager include:
- Direct the planning, execution, and oversight of Phase I-IV clinical trials, ensuring studies are delivered on schedule, within budget, and in compliance with regulatory requirements.
- Serve as the primary liaison between sponsors, CROs, clinical sites, vendors, and cross-functional stakeholders to drive study objectives and milestones.
- Monitor trial progress, identify operational risks, and implement mitigation strategies to maintain study quality and performance.
- Oversee study timelines, enrollment metrics, vendor activities, and financial tracking to support successful clinical program execution.
- Lead cross-functional study teams and provide strategic guidance throughout protocol implementation, database lock, and study closeout activities.
- 8+ years of clinical project management experience within biotechnology, pharmaceutical, or CRO environments.
- Proven experience managing clinical trials within Cardiovascular, MASH, Hepatology, Obesity, and/or Dermatology therapeutic areas.
- Strong knowledge of ICH-GCP guidelines, FDA regulations, and global clinical trial operations.
- Experience managing CROs, vendors, budgets, timelines, and multinational clinical studies.
- Bachelor's degree required; advanced degree in Life Sciences, Public Health, Nursing, or a related discipline preferred.
- $160,000 - $175,000 annually plus bonus
- Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.
- Fully remote work environment.
- This job opens for applications on 10/9/2026. Applications for this job will be accepted for at least 30 days from the posting date.