Seeking a highly organized, detail-oriented Clinical Research Coordinator to join our team and bridge the gap between innovative medical research and compassionate patient care.
As the Clinical Research Coordinator, you will manage the daily operations of our clinical trials. You will work closely with our Principal Investigators (PIs), clinical staff, and industry sponsors to ensure that all research is conducted with the highest degree of integrity, compliance, and patient safety.
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.
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- Exceptional organizational skills with the ability to manage multiple protocols simultaneously.
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- Professional demeanor, high ethical standards, and a "patient-first" mentality.