Job Title: Clinical Project Manager (CPM)
Location: Raleigh/Durham, NC (Hybrid - 3 days onsite per week)
Company Overview:
Join a dynamic and rapidly expanding organization with 7-8 active sites in the Research Triangle Park (RTP) area. With a growing portfolio of 20+ ongoing studies and a pivotal site partnership on the horizon, this is an exciting opportunity to be part of a collaborative team at the ground floor.
At this fast-paced organization, every day brings new challenges and opportunities, and all employees have the potential to earn equity shares in the company.
Position Summary:
We are seeking a highly motivated Clinical Project Manager (CPM) to oversee study timelines, site management, and sponsor deliverables. This role offers a unique opportunity for professional growth with a pathway to Director-level responsibilities.
Key Responsibilities:
Lead the management of a newly awarded study with a three-week timeline.
Act as the primary liaison between sponsors and sites to ensure timely delivery of study milestones, including enrollment targets and KPIs.
Collaborate closely with clinical teams to monitor study progress and address site-specific needs.
Maintain strong relationships with sponsors and site staff to ensure seamless communication and problem resolution.
Work onsite at the RTP area sites three days per week, providing hands-on support and oversight.
Qualifications:
Experience Required: Proven expertise as a Project Manager within a Site Management Organization (SMO).
Strong ability to interface effectively with sponsors and site teams to ensure project success.
Knowledge of Regulatory Affairs: A foundational understanding is a plus.
Exceptional organizational and leadership skills with a hands-on approach to project delivery.
Location: Must be based in North Carolina.
Why Join?
Be part of a small, agile team (6-7 employees) driving meaningful change in clinical research.
Contribute to a company on the brink of transformative growth with potential for Director-level advancement.
Enjoy a dynamic work environment where every day offers variety and impact.
Receive equity shares at all levels of the organization.
Additional Opportunities:
We are also looking for a Regulatory Affairs Specialist (junior level) to support compliance and submissions.
If you are ready to join an innovative team and make a lasting impact in the clinical research space, let’s connect.
