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

Similar Jobs