The Clinical Research Coordinator II will independently coordinate advanced clinical research projects while ensuring strict adherence to federal and institutional regulations
Job Summary
The Clinical Research Coordinator II will independently coordinate advanced clinical research projects while ensuring strict adherence to federal and institutional regulations.
Responsibilities include screening potential subjects, managing study budgets, collecting monies, and performing specific protocol procedures like taking vital signs and ECGs.
The role requires maintaining the integrity of clinical trials by preparing IRB submissions, monitoring compliance, and assisting with operational and financial functions.
Matching Summary
The Clinical Research Coordinator II will independently coordinate advanced clinical research projects while ensuring strict adherence to federal and institutional regulations.
Skills & Requirements
Must-have
Licensed Registered Nurse in Tennessee
60 months patient care experience
Knowledge of IRB FDA OHRP GCP HIPAA regulations
Ability to work in stressful environment
Proficient with personal computer and databases
Nice-to-have
Travel nurse experience preferred
Prior clinical research experience preferred
Team oriented mindset
Keen judgment in evaluating information
Key Requirements
Graduated from accredited discipline specific program