Clinical Trial Site Navigator

Psi CRO; Tulsa (OK); On-site; USD 60,000 - 90,000; Full time

Job summary

Milestone One seeks a Site/Study Coordinator to support clinical trial activities at a medical institution. The role involves coordinating with the Sponsor or CRO, assisting with feasibility and recruitment, and ensuring protocol adherence across visits and data tasks.

Responsibilities include data entry into EDC systems, regulatory document preparation, site training, and collaboration with cross-functional teams to maintain study quality and compliance.

Qualifications

• Requires 2+ years coordinating clinical research studies involving human subjects.
• GCP certification required. IATA, CPR, Phlebotomy can be required or desirable.
• Certification in Clinical Research (ACRP or SOCRA) preferred or obtainable within 1 year.

Responsibilities

• Serve as primary liaison between Milestone One, Sponsor/CRO, and the medical institution.
• Assist feasibility assessment and provide timely responses to feasibility questions.
• Identify and evaluate patient recruitment and site eligibility for study inclusion.

Education

GCP

IATA

CPR

Phlebotomy Certification

ACRP/SOCRA Certification

Job description

Milestone One seeks a Site/Study Coordinator to support clinical trial activities at a medical institution. The role involves coordinating with the Sponsor or CRO, assisting with feasibility and recruitment, and ensuring protocol adherence across visits and data tasks.

Responsibilities include data entry into EDC systems, regulatory document preparation, site training, and collaboration with cross-functional teams to maintain study quality and compliance.