Clinical Research Coordin
$49,000–$70,000 year
On-site · Fairfax, Virginia, United States
Job Summary
The Clinical Research Coordinator leads recruitment efforts and screens potential patients for clinical studies, ensures enrollment targets are met, and processes all study-related documentation. Key responsibilities include obtaining informed consent, conducting study visits, entering data into EDC systems, and coordinating with clinical research associates to maintain accurate trial documentation. Applicants should have a Bachelor's degree in Science or a related field and at least 2 years of relevant experience. Proficiency in Microsoft Office and good clinical practice knowledge is essential.
Required Qualifications
- 2+ years’ relevant experience (e.g. research, clinical, interaction with study population, program coordination)
- Excellent Excel, Word, PowerPoint and reporting skills
- Excellent interpersonal skills to deal effectively with patients, physicians, clinicians and administrators
- Excellent organizational skills and self-management skills to independently manage work flow
- Ability to prioritize
- Meticulous attention to detail
- Knowledge of medical terminology
- Knowledge of good clinical practice, FDA, OHRP, HIPAA policies
- Ability to use EMR data as a subject recruitment tool
- Experience using Microsoft Office Suite, and clinical research systems (CTMS, Regulatory)
Desired Qualifications
- Certification through either ACRP or SoCRA highly preferred
Additional Requirements
- Equal Opportunity / Affirmative Action employer
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