Clinical Research Coordinator

A Nashville based research site is seeking a highly skilled Clinical Research Coordinator to manage the performance of clinical trials, ensuring compliance with federal regulations and company guidelines. The ideal candidate will promote best practices in clinical investigations, playing a critical role in the enrollment and maintenance of trial participants.

Primary Responsibilities:

• Study Management: The Clinical Research Coordinator will thoroughly understand all assigned studies by reviewing protocols, attending investigator and start-up meetings, and coordinating with the Principal Investigator.
• Protocol Adherence: They will strictly adhere to study protocols, obtaining necessary exemptions when required.
• Communication: The Coordinator will effectively communicate protocol issues to CROs, Sponsors, Site Administrators, and Principal/Sub-Investigators, documenting pertinent discussions via email or meetings.
• Patient Interaction: They will collect initial psychiatric and medical information through patient interviews and relevant sources, and educate patients and families about the study and clinical drug trials.
• Clinical Tasks: The Coordinator will perform clinical tasks, such as monitoring vital signs, performing ECGs, phlebotomy, and specimen packaging, while maintaining timely source documentation.
• Medication Management: They will dispense and maintain accurate records of study medications.
• Timely Queries: The Clinical Research Coordinator will address all monitor and sponsor queries promptly.
• Community Resources: They will provide appropriate referrals to community resources for patients and families at the conclusion of the study.

Knowledge, Skills, and Abilities:

• Outstanding verbal and written communication skills.
• Strong interpersonal and customer service skills.
• Excellent time management and organizational abilities.
• Demonstrated ability to foster mentoring relationships and drive organizational change.

Qualifications:

• High School Diploma or GED required; Bachelor’s degree strongly preferred.
• Minimum of two years’ experience in a clinical environment, with a focus on clinical research.
• LPN, RN, or other medical licensure or certification preferred.
• Strong working knowledge of GCP and FDA guidelines, as well as medical terminology.
• BLS Healthcare Provider certification required; bilingual candidates are preferred.

Why This Role? This position offers an exciting opportunity for a professional who is passionate about clinical research and committed to advancing healthcare. The Clinical Research Coordinator will be integral in driving innovative research and supporting patients throughout their clinical journey.

Apply now to join a team making a real difference in clinical trials!