What are the responsibilities and job description for the Clinical Research Coordinator position at Apex Clinical Studies?
Job Overview
Join Our Growing Clinical Research Team
We are seeking a motivated, organized, and patient-focused Clinical Research Coordinator (CRC) to join our fast-paced clinical research team. The ideal candidate is passionate about advancing medicine through clinical trials while providing exceptional patient care. This position offers opportunities to work on cutting-edge Phase I-IV clinical trials across multiple therapeutic areas, including obesity, vaccines, women's health, psychiatry, cardiology, gastroenterology, dermatology, pulmonology, neurology, and more.
Responsibilities
- Coordinate and manage clinical research studies from start-up through closeout.
- Screen, recruit, consent, and enroll study participants.
- Schedule and conduct study visits according to protocol.
- Collect, process, and ship laboratory specimens.
- Perform ECGs, vital signs, phlebotomy, and other protocol-required procedures (as applicable).
- Accurately document source data and complete electronic case report forms (eCRFs).
- Maintain regulatory binders and essential study documents.
- Ensure compliance with FDA regulations, ICH-GCP guidelines, sponsor requirements, and site SOPs.
- Coordinate with investigators, sponsors, CROs, laboratories, and study vendors.
- Report adverse events, protocol deviations, and safety information promptly.
- Prepare for sponsor monitoring visits, audits, and FDA inspections.
- Educate and support study participants throughout their trial experience.
- Meet enrollment goals while maintaining exceptional patient retention.
Qualifications
- Minimum 1 year of clinical research experience preferred.
- Knowledge of ICH-GCP, FDA regulations, and HIPAA.
- Experience with electronic data capture (EDC) systems and EMRs preferred.
- Phlebotomy and laboratory experience are a plus.
- Strong organizational and time-management skills.
- Excellent communication and interpersonal abilities.
- Bilingual a plus (English/Spanish).
- Ability to manage multiple studies simultaneously in a fast-paced environment.
Preferred Certifications
- GCP Certification
- CITI Human Subjects Protection Training
- HIPAA Training
- OSHA Bloodborne Pathogens Training (preferred)
- ACRP or SoCRA Certification (preferred but not required)
What We Offer
- Competitive salary
- Performance-based bonuses
- Paid time off and holidays
- Career growth opportunities
- Ongoing training and professional development
- Supportive team environment with opportunities to work on innovative clinical trials
- If you are passionate about improving patient lives and advancing medical research, we'd love to hear from you. Apply today and become part of a team dedicated to bringing tomorrow's treatments to patients today.
Pay: $15.00 - $35.00 per hour
Benefits:
- Paid time off
Work Location: In person
Salary : $15 - $35