Full-Time Lead Site/Study Coordinator
PSI CRO is hiring a remote Full-Time Lead Site/Study Coordinator. The career level for this job opening is Experienced and is accepting Remote based applicants remotely. Read complete job description before applying.
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PSI CRO
Job Title
Lead Site/Study Coordinator
Posted
Career Level
Full-Time
Career Level
Experienced
Locations Accepted
Remote
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Job Details
The Lead Site/Study Coordinator supports medical institutions for clinical trial activities. Support for staff is determined by the Principal Investigator.
Responsibilities:
Acts as a communication line between Milestone One Manager, medical institution staff, and Sponsor/CRO.
Ensures staff complete necessary training. Maintains study documents for visits/audits. Assists with regulatory documents and on-site staff training.
Reporting Lines:
Administratively reports to Milestone One Manager and to Principal Investigators for clinical trial responsibilities.
Education:
Associate Degree (Nursing preferred) with 5+ years of experience as a site/study coordinator.
Certifications:
Responsibilities:
- Assessing study feasibility
- Conducting research visits
- Assisting with scheduling and logistics
- Data entry into EDC systems
- Contacting CRO/sponsor representatives
- Compliance monitoring and mentoring
- Developing protocol-specific tools
Acts as a communication line between Milestone One Manager, medical institution staff, and Sponsor/CRO.
- Liaison for recruiting new site partners
- Resource for identifying new vendors
- Facilitates evaluation of proposed studies
- Identifies new projects within medical institution interests
- Participates in patient recruitment and eligibility confirmation
- Performs site quality checks
- Assists with plan development for recruitment/retention tools
- Evaluates protocols and develops recruitment strategies
- Provides training to Milestone One and site staff
- Assists in incorporating clinical trials into site practice
- Supports contract and budget negotiations
Ensures staff complete necessary training. Maintains study documents for visits/audits. Assists with regulatory documents and on-site staff training.
Reporting Lines:
Administratively reports to Milestone One Manager and to Principal Investigators for clinical trial responsibilities.
Education:
Associate Degree (Nursing preferred) with 5+ years of experience as a site/study coordinator.
Certifications:
- Current Good Clinical Practice (GCP)
- IATA
- CPR
- Phlebotomy certification (if not part of active licensure)
- Active Certification in Clinical Research (ACRP/SOCRA)
Skills
FAQs
What is the last date for applying to the job?
The deadline to apply for Full-Time Lead Site/Study Coordinator at PSI CRO is
16th of August 2025
. We consider jobs older than one month to have expired.
Which countries are accepted for this remote job?
This job accepts [
Remote
] applicants. .
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