Clinical Trials Site Coordinator

Psi CRO; Florida; On-site; USD 60,000 - 90,000; Full time

Job summary

Milestone One in Coral Springs, Florida, is seeking a Site/Study Coordinator to support a medical institution with clinical trial-related activities. You will assist in feasibility assessment, patient recruitment, data entry, regulatory submissions, and coordination with sponsors/CROs to ensure quality study conduct.

The role requires two years of experience coordinating clinical research, GCP/IATA/CPR certifications, and a focus on accurate documentation and regulatory compliance.

Qualifications

• Education and at least two years coordinating clinical research with human subjects.
• Current Good Clinical Practice (GCP) certification required or in progress.
• IATA and CPR certifications are preferred where applicable.

Responsibilities

• Act as a constant communication link between Milestone One, Sponsor or CRO, and the medical institution.
• Facilitate evaluation of proposed studies and ensure timely responses to feasibility questions.
• Participate in patient recruitment/identification and assess eligibility per criteria.
• Assist with development of recruitment tools, source documents, and site tools for quality and timing.
• Support obtaining informed consent and coordinating visits per protocol.

Skills

Communication

Organization

Attention to detail

Teamwork

Education

GCP Certification

IATA Certification

CPR Certification

Phlebotomy Certification

Clinical Research Certification (ACRP/SOCRA)

Job description

Milestone One in Coral Springs, Florida, is seeking a Site/Study Coordinator to support a medical institution with clinical trial-related activities. You will assist in feasibility assessment, patient recruitment, data entry, regulatory submissions, and coordination with sponsors/CROs to ensure quality study conduct.

The role requires two years of experience coordinating clinical research, GCP/IATA/CPR certifications, and a focus on accurate documentation and regulatory compliance.