Lead CRC II
Send a job offer directly to this candidate
Clinical Research Coordinator with 3+ years of experience managing Phase I-IV clinical trials across outpatient and inpatient settings. Experienced in study start-up, regulatory compliance, participant recruitment, source documentation, monitoring visits, audit readiness, and study closeout. Passionate about advancing clinical research through quality, efficiency, and patient-centered care while building strong relationships with sponsors, CROs, investigators, and study participants.
Lead Clinical Research Coordinator II
Managed 20+ clinical research studies across multiple therapeutic areas.
Led study start-up, regulatory submissions, IRB correspondence, monitoring visits, and study closeout.
Coordinated participant recruitment, informed consent, scheduling, data collection, and source documentation.
Maintained GCP, FDA, ICH, and protocol compliance while ensuring audit readiness.
Performed phlebotomy, specimen processing/shipping, investigational product accountability, and safety reporting.
Collaborated with sponsors, CROs, investigators, pharmacy, laboratory, and multidisciplinary healthcare teams.
Master of Science – Applied Life Sciences
Bachelor of Science – Anthropology
Certified Phlebotomy Technician I (CPT-I)
