Research Coordinator
Midlands Neurology & Pain Associate S.P.A. · Columbia, SC · 6 mo ago
On-siteAnalystFull-time
Key Responsibilities
- Oversee the lifecycle of clinical trials from site initiation to close-out.
- Screen, enroll, and consent eligible study participants; maintain high retention rates through excellent communication.
- Ensure accurate and timely entry of Case Report Forms (CRFs) and maintain meticulous regulatory binders.
- Adhere strictly to ICH-GCP guidelines, HIPAA regulations, and study-specific protocols.
- Perform or coordinate study-related procedures (vitals, phlebotomy, ECGs, and sample processing).
- Serve as the primary point of contact for Clinical Research Associates (CRAs) during monitoring visits and audits.
Qualifications
- Minimum of 2–3 years of experience in clinical research coordination.
- Bachelor’s degree in a life science, healthcare, or related field.
- CCRC or CCRP (ACRP/SoCRA) certification is highly preferred.
- Proficiency with Electronic Data Capture (EDC) systems and EMR platforms.
- Strong phlebotomy and laboratory processing skills.
- Exceptional organizational skills with the ability to manage multiple protocols simultaneously.
- Professional demeanor, high ethical standards, and a "patient-first" mentality.