Coordinator Clinical Research Oncology

OSF HealthCare • Peoria, IL

3d

About The Position

The Clinical Research Coordinator 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, this position 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. Also directs, and coordinates all aspects of research projects and is responsible for assuring research is conducted in an ethical manner, using Good Clinical Practice (GCP). Also responsible for both clinical and administrative/business functions relating to their assigned projects and play a critical liaison/connector role between study team, department leadership, Institution, Sponsors, and Institutional Review Board (IRB).

Requirements

• Bachelors in biological/life sciences or related field OR 2 years relevant clinical research experience
• Excellent interpersonal and communication skills.
• Solid computer skills, including proficiency with Microsoft software.
• Strong analytical and problem solving skills, with the ability to be detail oriented.
• Proficient in medical terminology

Nice To Haves

• Master's degree in clinical research, healthcare, sciences, business, or related field
• Clinical Research experience in Oncology
• 3 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
• IRB Rules/Regulations
• 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
• CPR certified through American Heart Association (AHA)

Responsibilities

• Reviews and comprehends the protocol.
• Supports, facilitates, and coordinates the daily clinical research/trial activities.
• Plays a critical role in the conduct of the study.
• Directs and coordinates all aspects of research projects.
• Ensures research is conducted in an ethical manner, using Good Clinical Practice (GCP).
• Responsible for both clinical and administrative/business functions relating to assigned projects.
• Plays a critical liaison/connector role between study team, department leadership, Institution, Sponsors, and Institutional Review Board (IRB).

Benefits

• comprehensive and market-competitive total rewards package that includes benefits, compensation, recognition and well-being offerings that focus on the whole person and engage with their current stage of life and career.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level