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Clinical Research Coordinator

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Onsite

Clinical Research Coordinator

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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