C
ClinLab Solutions Group
Clinical Research Coordinator
Skills
Data AnalysisComplianceRegulatory Compliance
2 months ago
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Important information
Contract type:
Permanent
Location:
Savannah, GA, USA
Work mode:
Onsite
Published on:
18 August 2026
What they need
Essential Responsibilities and Duties:
- Coordinates patient-related activities for complex and/or multiple studies under supervision, from study startup through close-out.
- Maintains and organizes clinical trial research documentation.
- Monitors study subjects and supports data analysis and reporting.
- Coordinates the timing and collection of study data.
- Identifies, documents, and reports adverse events, protocol deviations, and other unanticipated problems through the appropriate channels.
- Tracks and reports research data to uphold quality and regulatory compliance.
- Completes study-related administrative and regulatory tasks as needed.
- Contributes to protocol development activities.
- Confirms the site receives accurate information and materials from sponsors (e.g., source documents, protocol, scales, supplies, approvals, contacts).
- Explains protocol-specific requirements and expectations to prospective participants and their caregivers.
- Conducts protocol-required safety and efficacy assessments (vital signs, EKGs, blood draws, and other assigned procedures).
- Supports the Clinical Trial Manager (CTM) in overseeing vendors, accounting, regulatory matters, client satisfaction, recruitment, quality, and trial outcomes.
- Assists the CTM with planning, process development, staff training, and team development.
- Takes on additional duties as assigned. The responsibilities above describe the general level and nature of work for this role and are not intended to be all-inclusive.
Education / Experience / Skills:
- Proven experience and demonstrated proficiency as a Clinical Research Coordinator.
- High school diploma or equivalent required; Bachelor's degree preferred.
- CCRC certification preferred.
- 2–3 years of experience in the medical field preferred.
- Working knowledge of federal regulations governing the protection of human research subjects and the conduct of clinical trials.
- Strong leadership and mentorship abilities.
- Skilled at building and maintaining effective working relationships across all levels of the organization, as well as with sponsors and vendors.
- Sound crisis management and problem-solving skills, with the ability to stay calm and effective under pressure.
- Works well both independently and as part of a team.
- Strong verbal and written communication skills.
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