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Career Center
Clinical Research Coordinator Position
Job Description
Responsible for study related procedures for clinical trials in a large Gastroenterology Practice. This includes ECG, lab work, preparing specimens for shipping, vital signs and scheduling subject exams with investigators. Report to Senior Clinical Research Coordinator who is a Nurse Practitioner. Periodic travel to investigator’s meetings is also required. Position is autonomous and duties include:
·Performing all procedures in compliance with FDA, IRB, GCP and ICH regulations and guidelines
·Recruit and enroll study patients from within practice with chart reviews and with use of marketing strategies
·Follow subjects throughout all study visits
·Maintain all study files and CRFs
·Maintain screening enrollment and drug accountability logs
·Meet with Senior Clinical Research Coordinator to ensure communication and quality of data
·Prepare for monitoring and auditing visits
·Assist with drafting policies and procedures as needed.
Required Experience
At least 1 year experience as a Clinical Research Coordinator. Demonstrates a strong attention to detail with superior organizational skills. Computer skills with EDC experience, and good communication skills a must. A strong knowledge of commitment and adherence to FDA and IRB regulations necessary. Must work as a team member and exhibit flexibility.
Education Requirements
Nursing training or other form of medical certification preferred. CCRC certification beneficial, but not required.
Contact details:
GASTROENTEROLOGY RESEARCH ASSOCIATES,
L.L.C.
65 RIDGEDALE AVENUE
CEDAR KNOLLS, NJ 07927