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Clinical Research Coordinator CRC / LPN / RN
| Details |
Country: USA
Location: Colorado-Denver Denver, CO 80220
Total applied: 35 Salary/Wage:Very competitive salary commensurate with experience, excellent benefits, and incentives.
Job Category:Medical/Health
Relevant Work Experience:1+ to 2 Years
Education Level:Bachelor's Degree
Location:Denver, CO 80220
Status:Full Time, Part Time, Employee
Occupations:Nursing;General/Other: Medical/Health;Physician's Assistant/Nurse Practitioner
Career Level:Experienced (Non-Manager)
Relevant Work Experience:1+ to 2 Years
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Clinical Research Coordinator CRC / LPN / RN
A fast growing multidisciplinary research center is currently seeking an experienced clinical research coordinator to join our staff. Qualified candidates must be a licensed practical nurse or registered nurse and have a minimum of 1 to 2 years of experience in conducting clinical trials according to the FDA and GCP/ICH guidelines. Any additional training will be provided.
Requirements: CCRC certification preferred but not required, proficiency in both Spanish and English required.
This position also requires excellent communication, organizational and time-management skills, attention to detail and able to work independently as well as collaborate with a team.
General responsibilities include:
· Demonstrate working knowledge and understanding of assigned clinical trial protocols.
· Conduct clinical trials, including but not limited to recruitment, screening, enrollment, and follow up of eligible subjects according to protocol requirements.
· Complete all study documentation including but not limited to regulatory documents, drug dispensing log, subjects log, study-related communication, detailed source documentation and timely case report form completion.
· Coordinate and conduct patient care visits and assure all procedures are conducted in compliance with the clinical protocol and company standard operating procedures.
· Work closely with principal investigator to assure, when needed, subjects receives appropriate medical evaluation and care, alerting the principal investigator and site director of serious adverse events
· Serve as liaison with investigators, study sponsors, CROs, IRBs, monitors, and other health care providers, to ensure successful and safe conduct of assigned studies.
· Attend sponsor Investigator meetings as needed for assigned clinical trials.
· Conduct clinical research in compliance with ICH and GCP guidelines
· Collaborate with recruitment, planning and implementation.
This full time position offers a competitive salary commensurate with experience, excellent benefits, and incentives.
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