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Expected pay for the Coordinator of Clinical Research II is $31.49 - $37.05/hour.
Expected pay for the Clinical Research Coordinator is $29.30- $34.47.
Actual pay will be determined by experience, skills and internal equity. This is a Salaried position.
Overview
This position does not offer H1B Sponsorship.
POSITION SUMMARY:
The Clinical Research Coordinator II (CRC II) is a specialized research professional working with, and under the direction of the Principal Investigator (PI). While the PI is primarily responsible for the overall design, conduct, and management of the research studies, the CRC II supports, facilitates and coordinates the daily clinical research activities and plays a critical role in the conduct of the research at the institution.
The CRC II must exhibit a moderate level of expertise in the conduct of clinical research and will complete most research tasks independently with minimal direction. The CRC II in collaboration with the PI is responsible for assuring research is conducted in an ethical manner and all study activities are completed by strictly following Good Clinical Practices (GCP). The CRC II is responsible for both clinical and administrative business functions relating to their assigned projects and play a critical liaison role between study team, department leadership, Institution, Sponsors, and Institutional Review Board (IRB).
**This position will be located on site at St. Francis Medical Center in Peoria, IL.**
Qualifications
CRC II REQUIRED QUALIFICATIONS:
Education/Experience:
Bachelor's degree
OR High School Diploma and 4 years of experience in clinical research
Other Licenses/Certifications:
Certified Clinical Research Coordinator (CCRC) OR Certified Clinical Research Profesisonal (CCRP)
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:
Experience: 2 years direct clinical research experience that includes interventional clinical trial experience.
Strong Project Management Skills Understanding of research regulations (e.g. IRB, FDA, OHRP, GCP, etc.
Experience with electronic health records and data capturing systems. Other requirements/information: Proficient in medical terminology
Clinical Research Coordinator REQUIRED QUALIFICATIONS:
Education: Bachelor Degree 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: 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.