Clinical Project Manager - Evidence Generation

Job Title: Evidence Generation Project Manager / Project Lead (Full-Time Contract)

Location: Remote
Reports To: Director of Evidence Generation

Position Summary:
We are seeking a highly organized and proactive Evidence Generation Project Manager / Project Lead to oversee the operational execution of our post-marketing clinical trials. The ideal candidate will have strong project management skills in clinical research, with a proven ability to manage multiple studies simultaneously in a fast-paced environment. This role is critical for ensuring that all post-marketing studies-including Phase 4 trials, real-world evidence (RWE) studies, and health economics and outcomes research (HEOR) projects-are executed efficiently, on time, and aligned with organizational objectives.

Key Responsibilities:

• Manage and oversee all operational aspects of post-marketing clinical trials, ensuring adherence to timelines, budgets, and regulatory requirements.

• Develop, maintain, and continually optimize project trackers, dashboards, and reporting tools to monitor progress across multiple studies.

• Coordinate cross-functional execution at all levels to support evidence generation initiatives.

• Track and accelerate recruitment timelines, identifying and resolving bottlenecks to ensure study targets are met.

• Provide day-to-day project management support, including risk identification, issue resolution, and escalation when necessary.

• Serve as a central point of contact for all project-related communications, facilitating collaboration among internal teams, vendors, and clinical sites.

• Support the Director of Evidence Generation with strategic planning and operational execution.

• Lead projects without direct authority, demonstrating strong influencing skills and the ability to align stakeholders toward common goals.

Qualifications:

• 2-5 years of clinical trial project management experience, preferably with experience in post-marketing or Phase 4 studies.

• Demonstrated ability to manage multiple concurrent clinical trials (8-10 studies) in a fast-paced environment.

• Strong proficiency in project management tools, trackers, and reporting dashboards.

• Excellent organizational, communication, and interpersonal skills, with the ability to lead cross-functional teams without formal authority.

• Detail-oriented, proactive, and solution-focused, with strong problem-solving capabilities.

• Experience with RWE, HEOR, and post-marketing study operations is a plus.

Why You'll Love This Role:

• Opportunity to work on multiple impactful post-marketing clinical trials and evidence generation projects.

• Fast-paced environment with exposure to innovative clinical strategies and real-world data initiatives.

• Collaborative team culture with opportunities for professional growth and skill development.