Job Description
**Seeking a Clinical Research Coordinator (CRC) in Nashville, TN to join a dynamic research team. The CRC will be responsible for performing a variety of clinical research tasks to support multiple protocols and ensure the highest standards of patient care, compliance, and data integrity.**
Job Title: Clinical Research Coordinator (CRC)
Location: Nashville, TN
Employment Type: Contract (1040 hours) with possible extension.
Schedule: Monday-Friday 7am-4pm or 8am-5pm
Start Date: ASAP
Duties Include but Are Not Limited To:
- Practice and adhere to the organization’s Code of Conduct and Mission and Value Statement.
- Complete all assigned training by designated due dates.
- Perform routine operational activities across multiple clinical research protocols.
- Act as a liaison between site research personnel, industry sponsors, and supervisor.
- Collaborate with internal departments (finance, hospital administration, IRB) to ensure smooth study operations.
- Coordinate schedules from study feasibility through study closeout.
- Review study design and patient eligibility criteria with physicians and patients.
- Ensure patient safety and protocol compliance through accurate informed consent procedures.
- Maintain data integrity by thorough source document review and timely, accurate data entry into Case Report Forms (CRFs) or Electronic Data Capture (EDC) systems.
- Create study-specific source documentation tools when needed.
- Track and report adverse events, serious adverse events, protocol deviations, and violations.
- Manage study supplies, drug/device shipments, and inventory.
- Attend study-specific meetings, investigator meetings, conference calls, and CRC team meetings as required.
- Review and respond to monitoring and audit findings.
Knowledge:
- Organizational policies, Standard Operating Procedures (SOPs), and clinical research systems.
- Emerging understanding of ICH Guidelines and the Code of Federal Regulations (CFR).
- Basic medical terminology.
Skills:
- Strong communication, organizational, and time management skills.
- Basic clinical procedures, including ECG acquisition, phlebotomy, specimen handling, storing, and shipping.
Abilities:
- Strong interpersonal skills and ability to work collaboratively.
- Highly self-motivated with meticulous attention to detail.
Clinical Competencies:
- Required to perform clinical tasks such as ECGs, phlebotomy, and specimen processing.
- Training and/or certification will be provided as necessary per study protocols.
Must-Have Qualifications:
- Bachelor’s Degree.
- Minimum 2 years of Clinical Research Coordinator (CRC) experience within the last 2 years.
- Phlebotomy experience.
Why Join Us?
- Grow your career in an evolving and high-demand field.
- Work with a dedicated, supportive team environment.
- Make a real impact on patient care and scientific advancement.
Interested candidates:
Apply today to join an industry leader in clinical research excellence!
Job Tags
Contract work, Immediate start, Monday to Friday,