The Clinical Research Coordinator (CRC) is a specialized research professional working with, and under the direction of a clinical Principal Investigator (PI). While the PI is primarily responsible for the overall design, conduct, and management of the research project/trial, the CRC reviews and comprehends the protocol and supports, facilitates, and coordinates the daily clinical research/trial activities and plays a critical role in the conduct of the study. The CRC plans, directs, and coordinates all aspects of research projects. CRC is responsible for assuring research is conducted in an ethical manner, using Good Clinical Practice (GCP). CRC’s are responsible for both clinical and administrative/business functions relating to their assigned projects. CRC’s play a critical liaison/connector role between study team, department leadership, Institution, Sponsors, and Institutional Review Board (IRB).
Bachelor’s degree in biological/life sciences or related field or 2 years relevant clinical research experience
Proficient in Microsoft Word, Excel, Power Point, and general computer proficiency required.
Strong organization skills: ability to multi-task, prioritize and meet deadlines. Must demonstrate attention to detail and accuracy, time management skills, and proven ability to successfully follow-through on multiple, assigned projects.
Professional and effective verbal and written communication skills and strong interpersonal skills, with the ability to work and communicate with various individuals within and external to the organization.
Proficient in medical terminology.
Collaborative Institutional Training Initiative (CITI) Training Course Certificates: Human Subject Protection (HSP), Good Clinical Practice (GCP), Responsible Conduct of Research (RCR), Conflict of Interest (COI)
Certified Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP)
International Air Transport Association (IATA) – Shipping of Dangerous Goods certification from Mayo Clinic
Master’s degree in clinical research, healthcare, sciences, business, or related field
3-4 years direct research experience in a study coordinator role
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e., International Conference on Harmonization (ICH), Good Clinical Practice (GCP) and CFR 21.
1 year phlebotomy experience
Job seekers will be afforded equal opportunity regardless of their race, ethnicity, veteran status or disability status.
Experience the OSF culture and community by clicking here.