Clinical Research Coordinator

About the Role

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We are looking for a proactive and detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical research studies in compliance with Good Clinical Practice (GCP), institutional policies, and federal regulations. In this role, you will collaborate with investigators, sponsors, and study participants to ensure accurate execution of study protocols and high-quality data collection.

 

Key Responsibilities

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• Coordinate and conduct day-to-day study activities, including participant recruitment, informed consent, scheduling, and follow-up.

• Ensure strict adherence to study protocols, FDA, IRB, and ICH-GCP regulations.

• Accurately collect, record, and enter study data into electronic data capture (EDC) systems.

• Maintain complete and organized study documentation, including regulatory binders, subject files, and case report forms.

• Identify, document, and report adverse events, ensuring timely communication with IRBs and sponsors.

• Prepare for and actively participate in monitoring visits, audits, and regulatory inspections.

• Work closely with multiple principal investigators, sponsors, community partners, local clinics and research staff to ensure smooth study operations.

 

Qualifications

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• Bachelor’s degree in health sciences, life sciences, nursing, or a related field (required).

• 1–3 years of clinical research experience (preferred).

• Fluency in Spanish is strongly preferred

• Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) is preferred.

• Phlebotomy certification with demonstrated ability to draw, process, and ship specimens in compliance with IATA guidelines

• Strong understanding of GCP, FDA , and IRB regulations.

• Excellent organizational, communication, and problem-solving skills.

 

What We Offer

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• Dental insurance

• Flexible schedule

• Health insurance

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