Job detail

Coordinator Clinical Research Oncology

OSF HealthCare

#CPR #Phlebotomy #Medical Terminology #Clinical Research #Principal Investigator #GCP #Clinical Trial #ICH #Oncology

Quick overview

The coordinator supports the Principal Investigator by managing daily clinical trial activities and ensuring research is conducted ethically according to GCP standards. They serve as a critical liaison between the study team, sponsors, and the Institutional Review Board.

Requirements summary

Requires a Bachelor's degree in biological/life sciences or 2 years of relevant clinical research experience. Preferred candidates possess a Master's degree, oncology research experience, and certifications such as CCRC or CCRP.

bachelor degreepostgraduate degreeprofessional certificateInterpersonal CommunicationPhlebotomyMedical TerminologyMicrosoft Office ProficiencyClinical Research CoordinationGood Clinical Practice (GCP)Analytical Problem SolvingProtocol ReviewOncology ResearchIRB Regulations

Job description

Total Rewards

"Your life - our Mission" OSF HealthCare is dedicated to provide Mission Partners with a 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.
Click here to learn more about benefits and the total rewards at OSF.
Expected pay for this position is $29.30 - $34.47/hour.
Actual pay will be determined by experience, skills and internal equity.
This is a Salaried position.

Overview

**Please note H1B Sponsorship is not available for this position.**

Position Summary

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).

Qualifications

Required qualifications

Education: Bachelors in biological/life sciences or related field
OR 2 years relevant clinical research experience
Other skills/knowledge: 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.

Preferred Qualifications

Education: Master's degree in clinical research, healthcare, sciences, business, or related field Experience: Clinical Research experinece 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 Licensure/Certifications: 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) Other requirements/information: Proficient in medical terminology OSF HealthCare is an Equal Opportunity Employer.