Onsite Clinical Research Coordinator I - Nashville

Regulatory Jobs

Nashville (TN)

On-site

USD 42,000 - 60,000

Full time

7 days ago
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Job summary

ICON's Accellacare team in Nashville, TN is seeking a Clinical Research Coordinator 1 to support study coordination and ensure participant safety onsite at 5653 Frist Blvd. The CRC 1 will perform protocol-driven procedures, recruit participants, attend investigator meetings, and maintain accurate data and logs while promoting the site to sponsors.

This onsite role requires strong attention to detail, good time management, and a commitment to integrity and quality in clinical research.

Qualifications

  • 1+ years of work experience in a clinical research or pharmaceutical environment.
  • Strong attention to detail.
  • Motivated about a career in clinical research.
  • Excellent time management and planning skills with an organized approach to work.
  • Bachelor's degree in life sciences or other related field.

Responsibilities

  • Perform protocol-specific clinical procedures as ordered by the investigator.
  • Attend investigator meetings and site visits for training.
  • Recruit and promote services to suitable participants and sponsor representatives.
  • Document data, logs, and adverse events accurately.
  • Prepare study documentation for audits.
  • Order and manage supplies and drug administration as required.
  • Maintain temperature monitoring and equipment calibration.

Skills

Clinical research experience
Attention to detail
Time management
Organized
Motivated to a career in clinical R&D

Education

Bachelor's degree in life sciences or related field

Job description

ICON's Accellacare team in Nashville, TN is seeking a Clinical Research Coordinator 1 to support study coordination and ensure participant safety onsite at 5653 Frist Blvd. The CRC 1 will perform protocol-driven procedures, recruit participants, attend investigator meetings, and maintain accurate data and logs while promoting the site to sponsors.

This onsite role requires strong attention to detail, good time management, and a commitment to integrity and quality in clinical research.

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