Details:

  • Compensation: $50,000 - $70,000k
  • Benefits: Medical, Dental, Vision
  • Employment Classification: Direct Hire
  • Status: On-Site
  • Job ID: 21545

Job Title: Clinical Research Coordinator

Work Location: Broward County, Florida

Summary:

Seeking a Clinical Research Coordinator to support clinical trial operations, participant management, and regulatory compliance. This role involves direct interaction with study participants, data management, and collaboration with research partners. Ideal candidates will have a background in life sciences or healthcare, relevant certifications, and a commitment to professional stability.

Responsibilities:

  • Recruit and enroll study participants in accordance with study protocols and regulatory guidelines.
  • Conduct and document study visits, including obtaining informed consent, collecting vitals, and performing study-specific procedures.
  • Maintain accurate and audit-ready source documentation and enter data into case report forms.
  • Communicate with regulatory bodies and research partners to ensure compliance and manage study correspondence.
  • Coordinate participant scheduling, follow-up visits, and retention activities to support study continuity.
  • Assist with site initiation, monitoring, and close-out visits as required by study protocols.
  • Manage investigational product accountability and ensure proper handling and documentation.
  • Identify, document, and report adverse events and protocol deviations in a timely manner.

Qualifications:

  • Bachelor's degree in life sciences, health sciences, nursing, or a related field.
  • Up to 2 years of experience in clinical research or direct patient care (entry-level candidates considered).
  • Knowledge of ICH/GCP guidelines and FDA regulations.
  • Experience with electronic data capture systems such as Medidata Rave, REDCap, or similar platforms.
  • Phlebotomy and basic clinical procedures experience preferred.
  • Demonstrated professional stability in previous roles.
  • CITI Human Subjects Research and CITI GCP for Clinical Trials certifications (required).
  • ACRP CCRC or SoCRA CCRP certification preferred; candidates actively pursuing certification will be considered.
  • BLS/CPR certification required or obtainable upon hire.

Published Category: Clinical Operations & Development

Apply to this Position:

Include a message to the recruiters.
Attach a Resume file. Accepted file types are DOC, DOCX, PDF, HTML, and TXT.

We are uploading your application. It may take a few moments to read your resume. Please wait!