Clinical Research Coordinator ~ Contract $25-$30/hr in Columbus, OH at Vaco

Date Posted: 10/8/2020

Job Snapshot

Job Description

Clinical Research Coordinators - don't let your resume get lost in the shuffle!

Let Vaco serve as your advocate in presenting you to our top clients who are looking for CRC professionals. Our clients have immediate opportunities for Clinical Research Coordinators; don't let your resume get lost in the shuffle - let us work for you! At Vaco, we give you an advantage over your competition! Our recruiters have direct relationships with hiring managers, so they can connect your work experience to the open job-promoting your strengths to the manager while preparing you for that specific interview.

Our recruiters will provide you with great insight about trends in the industry - keeping you up to date on compensation expectations, company culture, and growth opportunities. If your background is in accounting as an CRC and you want to partner with the best, apply today!

As a Clinical Research Coordinator, you will coordinate and implement clinical research under the direction of the Principal Investigator.

Additional responsibilities of the CRC include:

  • Planning and directing clinical research projects and trials
  • Screening potential trial participants through interviews, medical records reviews, and follow-ups with doctors and nurses
  • Maintaining precise records of research activity to include case reports, informed consent forms, regulatory forms, drug dispensation records, and so on
  • Monitoring ongoing research activity to maintain compliance with scientific protocols and government regulations

Job Requirements

Requirements for the Clinical Research Coordinator position: • Previous experience as a CRC is required • Able to read, analyze, and interpret information from professional journals, technical procedures, or governmental regulations • Able to effectively present information and respond to questions from physicians, staff and patients • Knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research required • Knowledge of medical terminology, clinical medicine, clinical trials and GCP concepts