Serve as the primary sponsor contact for assigned U.S. clinical trial sites, ensuring consistent, responsive communication throughout study execution.
Build strong relationships with investigators and site staff to support site engagement, trial readiness from start up to close out, and sustained study performance.
Deliver training to site personnel on study protocols, operational requirements, study objectives, and the scientific rationale for investigational products.
Partner with sites to support patient recruitment and retention strategies, helping to identify barriers and opportunities to improve enrollment.
Collaborate closely with Clinical Operations and CRO partners to identify, address, and escalate operational or compliance issues in a timely manner.
Conduct remote and in-person site visits to strengthen site relationships, gather feedback, provide sponsor oversight and support effective trial execution.
Capture and communicate actionable insights from sites to inform study operations, enrollment planning, and protocol execution.
Contribute to feasibility assessments and site selection activities by sharing knowledge of local treatment practices, site capabilities, and patient access considerations.
Support consistent execution across assigned sites by reinforcing study expectations, compliance standards, and best practices.

Requirements

Bachelor’s degree in a scientific, healthcare, or related field required. Advanced degree preferred but not required.
6+ years of clinical trial experience in the pharmaceutical, biotech, or CRO industry, including strong knowledge of clinical operations and study conduct.
Previous experience working in a clinical trial liaison role or role with similar scope.
Demonstrated experience working directly with investigators, site staff, and cross-functional clinical teams to support study delivery and enrollment goals.
Working knowledge of GCP, ICH guidelines, and U.S. regulatory requirements.
Ability to independently manage multiple sites and priorities while exercising sound judgment in a dynamic environment.
Strong communication, collaboration, problem-solving, and relationship-building skills.
Experience using clinical trial systems such as IRT, EDC, and eTMF.
Willingness and ability to travel up to 60% for site engagement, meetings, and study-related activities.

Benefits

Annual bonus
Equity compensation
Competitive benefits package

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical trial experienceclinical operationsstudy conductGCPICH guidelinesU.S. regulatory requirementssite selectionfeasibility assessmentspatient recruitmentstudy protocols

Soft Skills

communicationcollaborationproblem-solvingrelationship-buildingindependent managementsound judgmentadaptabilitytraining deliveryengagementfeedback gathering