Senior Clinical Project Manager

Jobgether

4d • Hybrid

About The Position

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Clinical Project Manager in the United States.
This role provides an opportunity to lead and manage complex clinical trials from start-up through study closeout in a fast-paced, global environment. The Senior Clinical Project Manager will oversee multi-center, multi-national projects, ensuring timelines, budgets, and quality standards are met while facilitating cross-functional collaboration. You will have direct influence on clinical trial strategy, patient recruitment, and operational execution, contributing to the development of innovative treatments for oncology and rare diseases. The position combines hands-on project management with leadership, mentoring, and problem-solving responsibilities. Ideal candidates are detail-oriented, proactive, and thrive in dynamic settings where critical thinking and adaptability are essential. This role also offers exposure to international regulatory requirements and strategic clinical operations.

Requirements

• Bachelor’s degree in life sciences required; PMP preferred.
• 5+ years of experience in clinical trial project management, with late-phase (Phase 3–4, registration) trial experience preferred.
• Strong knowledge of ICH Good Clinical Practice (GCP) and regulatory processes.
• Experience managing global, multi-center clinical trials, preferably in oncology or radiopharmaceuticals.
• Excellent oral and written communication, organizational, and problem-solving skills.
• Demonstrated leadership capabilities and ability to develop team members.
• Proficiency in Microsoft Office Suite and electronic record-keeping systems.
• Ability to adapt to changing priorities, think creatively, and solve complex problems in a fast-paced environment.
• Inclusive mindset, ethical behavior, and commitment to continuous learning and results-oriented execution.

Responsibilities

• Lead all phases of clinical trial management, including vendor selection, site feasibility, protocol implementation, and study closeout.
• Develop and maintain integrated project management plans and timelines, ensuring alignment with study objectives and regulatory standards.
• Oversee budgets, contracts, and resources for trials, including negotiations with sites and vendors.
• Monitor external partners’ performance to ensure quality, timelines, and budgets are adhered to.
• Manage risk proactively, resolving issues and providing solutions to maintain study progress.
• Support the development and maintenance of clinical SOPs and trial processes.
• Mentor and train junior clinical project managers, fostering team development and knowledge sharing.
• Develop patient recruitment strategies and engage with investigators at medical conferences and meetings.
• Ensure regulatory compliance across regions, including APAC, EMEA, and North America.

Benefits

• Competitive salary and annual performance-based bonus.
• Equity-based incentive program.
• Generous vacation and paid wellness days.
• Support for professional learning and development.
• Flexible work arrangements, including hybrid and remote opportunities.
• Collaborative, global, and interdisciplinary team environment.
• Opportunity to contribute to life-changing oncology and rare disease clinical programs.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level