Research Coordinator Position Available In Clay, Florida

Research Coordinator

PHYSICIANS GROUP SERVICES, PA – 3.7

Orange Park, FL Job Details Estimated:

$49.7K – $69.3K a year 1 day ago Benefits Paid holidays Disability insurance Health insurance Dental insurance 401(k) Paid time off Vision insurance Opportunities for advancement Life insurance Qualifications Research Mid-level Bachelor’s degree Clinical trials 2 years Communication skills Full Job Description Join Our Team at Coastal Health!

Position:

Clinical Research Coordinator Location:

[Insert Location, if applicable] Coastal Health is currently seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic and growing team. In this role, you’ll play a vital part in the successful conduct of clinical trials, supporting Coastal Clinical Research Specialists’ mission to advance health through high-quality research practices.

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for managing all aspects of assigned clinical trials, ensuring compliance with all federal, state, local, and institutional regulations, as well as Coastal’s Standard Operating Procedures (SOPs). The CRC will provide patient care and perform administrative duties in support of research protocols while ensuring participant safety and data integrity.

Benefits Include:

Competitive wages Health, dental, vision, and life insurance Short & long-term disability coverage 401(k) retirement plan Up to 3 weeks paid time off 7 paid holidays Opportunities for professional growth and career advancement

Key Responsibilities:

Ensure thorough knowledge and compliance with all assigned clinical protocols Coordinate and attend investigator and staff protocol training sessions Screen, enroll, and follow-up with research participants according to protocol guidelines Ensure IRB approval and proper informed consent procedures are followed Conduct clinical assessments and procedures such as vital signs, ECGs, phlebotomy, and specimen handling Maintain accurate and timely documentation in source records and Case Report Forms (CRFs/eCRFs) Manage investigational product inventory and accountability Communicate effectively with physicians, patients, sponsors, CROs, and regulatory bodies Participate in monitoring visits and respond to queries promptly Maintain certifications and proficiency in protocol-required rating scales Ensure compliance with

GCP, IRB

requirements, and

Coastal SOPs Qualifications:

Bachelor’s degree in a health, science, or research-related field Minimum of 2 years of experience in a research or healthcare setting Strong attention to detail with excellent organizational and documentation skills Professional verbal and written communication abilities Ability to work independently and manage multiple priorities Skilled in establishing rapport with patients and maintaining professional interactions Familiarity with clinical trial protocols, informed consent processes, and regulatory requirements If you’re passionate about clinical research and are looking for a place to grow professionally while making a difference in healthcare, we’d love to hear from you. Apply today and become a part of Coastal Health’s mission to deliver impactful research and exceptional patient care! Bachelors degree in health, science or research-related field Two years experience in research or healthcare environment Detail-oriented individual with the ability to collect, document and analyze information Demonstrate professional communication (written and verbal) Demonstrate ability to establish rapport and maintain professional interaction skills Ability to communicate research protocol requirements effectively to potential trial participants and team members Ability to work independently, manage time effectively, prioritize tasks and work efficiently