Clinical Research Coordinator (CRC)
Behavioral Health Market Context
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Benefits
Competitive salary (based on experience)Benefits PackageESOPOpportunities for growth within a rapidly expanding research siteSupportive and collaborative team environmentExposure to cutting-edge clinical trials401(k)401(k) matchingDental insuranceEmployee assistance programFlexible spending accountHealth insuranceHealth savings accountLife insurancePaid time offRetirement planVision insurance14 more items(s)
Qualifications
- •Medical Assistant (MA) or Nursing experience required
- •Knowledge of GCP, FDA regulations, and clinical trial processes
- •Strong organizational skills and attention to detail
- •Ability to multitask in a fast-paced environment
- •Excellent communication and patient-facing skills
- •Graduate of an accredited Medical Assistant program, Nursing program, or related healthcare training required
- •3 more items(s)
Responsibilities
- •The CRC will play a critical role in the day-to-day execution of clinical trials, ensuring compliance with protocol requirements, FDA regulations, and ICH-GCP guidelines
- •Coordinate and execute clinical trials from startup through closeout
- •Screen, recruit, and consent study participants
- •Schedule and conduct study visits in accordance with protocol
- •Perform clinical procedures (vitals, ECGs, blood draws, specimen processing)
- •Maintain accurate and timely source documentation and data entry (EDC)
- •Manage investigational product accountability
- •Communicate effectively with sponsors, CROs, and site leadership
- •Ensure compliance with regulatory requirements and site SOPs
- •6 more items(s)
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