Clinical Research Coordinator at Headlands Research - ScoutJobs - The AI-curated global job board
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Posted 21 hours ago

Clinical Research Coordinator

Headlands ResearchClinical Research Coordinator

Perks & benefits

Annual LeaveHealth InsuranceMedical InsurancePaid Leave

Requirements

High school diploma or GED, 1+ year clinical trial coordination experience, Knowledge of FDA and ICH-GCP regulations, Proficiency in medical terminology, Microsoft Office proficiency

Skills

Clinical ResearchGCPEDC

About the role

Responsibilities

  • Coordinate all aspects of assigned clinical trials from site initiation to study close-out
  • Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards
  • Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs
  • Manage subject recruitment, informed consent, and retention strategies
  • Ensure timely data entry and resolution of EDC queries
  • Report and follow up on all adverse events, serious adverse events, and deviations
  • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems
  • Execute study procedures such as phlebotomy, ECGs, and sample processing within scope
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control

Requirements

  • High school diploma or GED required; Bachelor's Degree preferred
  • At least one full year of experience coordinating clinical trials phases 1-4
  • Familiarity with electronic data capture (EDC), IVRS, and other trial platforms
  • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
  • Proficiency in medical terminology and clinical documentation practices
  • Strong interpersonal, verbal, and written communication skills
  • Proficient in Microsoft Office and other clinical research systems

Preferred Qualifications

  • Industry-sponsored trial experience
  • Vaccine study experience
  • Hands-on clinical experience caring for patients with neurodegenerative diseases

Benefits

  • Competitive pay and annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays

About the Company

Headlands Research is a leading network of advanced clinical trial sites dedicated to enhancing clinical trial delivery and bringing innovative medical treatments to patients faster.

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Clinical Research Coordinator

Headlands Research · Plymouth

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