DPMG Clinical Research is a trusted leader in the medical research community, with a network of seven clinics dedicated to advancing science and patient care. Our strategically located sites provide access to a diverse patient population, further supported by our Street Medicine Program, which engages underserved communities to expand access and enhance recruitment. We are committed to conducting ethical, high-quality studies that drive medical progress and shape a healthier future for all.

Position Overview

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

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

Bachelors 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.

Work Environment

On-site role within a physician practice and clinical research setting.
Will involve handling biological samples and direct interaction with patients
Working in a fast-pace and rewarding environment of clinical research operations

Job Type: Full-time

Pay: From $23.00 per hour

Expected hours: 40 per week

Benefits:

Dental insurance
Flexible schedule
Health insurance