Research Trials Management Specialist

1 week ago


Nashville, Tennessee, United States K2 STAFFING LLC Full time

Job Overview:

K2 STAFFING LLC seeks an experienced Clinical Research Coordinator to manage clinical trials, adhering to federal regulations and company guidelines. This role promotes good clinical practices, collects documentation, and communicates protocol issues.

Key Responsibilities:

  1. Develop in-depth knowledge of assigned studies through protocols, investigator meetings, and coordination with the Principal Investigator.
  2. Ensure compliance with study protocols, obtaining exemptions when necessary.
  3. Effectively communicate protocol issues to relevant parties, including CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator.

Requirements:

  • High School Diploma or equivalent required; Bachelor's degree preferred.
  • Minimum two years of experience in a clinical setting; clinical research experience a plus.
  • LPN, RN, or related medical licensure/certification preferred.
  • Demonstrated understanding of GCP and FDA guidelines.
  • Familiarity with medical terminology.

Benefits Package:

  • Comprehensive insurance coverage, including medical, dental, vision, and flexible spending accounts.
  • 401(K) retirement plans with 4% employer match immediately vested.
  • Generous PTO policy and nine paid holidays.
  • A four-day workweek for full-time employees (Monday-Thursday).


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