About Us:
Tallahassee Research Institute is a leading research organization dedicated to advancing cardiovascular medicine through innovative research and clinical trials. We are seeking a highly motivated and experienced Clinical Research Coordinator to join our team.
Job Summary:
We are seeking a Clinical Research Coordinator to manage and coordinate cardiovascular clinical trials, primarily focused on device studies with some drug trials. The ideal candidate will have experience in clinical research, excellent communication skills, and the ability to work independently in a fast-paced environment. This is an on-site non-remote job.
Key Responsibilities:
- Manage and coordinate clinical trials from start-up to close-out, ensuring compliance with protocols, regulations, and institutional policies.
- Conduct patient recruitment, screenings, informed consent, and enrollment.
- Collect, review, and maintain accurate and complete source documents and case report forms and ensure accurate data entry.
- Coordinate with sponsors, investigators, and other research staff to ensure successful trial execution.
- Develop and maintain study-specific documentation, including study protocols, informed consent forms, adverse events, and study procedures.
- Ensure compliance with FDA regulations, ICH/GCP guidelines, and institutional policies.
- Participate in study initiation, monitoring, and close-out visits.
- Collaborate with the research team to identify and resolve study-related issues.
Requirements:
At least one of the following certifications/licenses is required:
- Certified Medical Assistant (CMA)
- Licensed Practical Nurse (LPN)
-Phlebotomy experience preferred but not required.
- Bachelor's degree in a life science, nursing, or related field is preferred but not required.
- Experience in clinical research is preferred, but we offer on-the-job training for the right candidate.
- Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Associate (CCRA) certification is a plus.
- Strong knowledge of FDA regulations, ICH/GCP guidelines, and clinical research principles is preferred.
- Excellent communication, organizational, and interpersonal skills are required.
- Ability to work independently and as part of a team.
What We Offer:
- Opportunity to work with a leading research organization in cardiovascular medicine.
- Collaborative and dynamic work environment.
- Professional development and growth opportunities.
- On-the-job training and certification support.
Please email resume to [email protected], and call 850-431-5024 with questions.
Job Type: Full-time
Benefits:
Schedule:
Ability to Commute:
Ability to Relocate:
Work Location: In person
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