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OSF HealthCare · 2 days ago

Clinical Research Coordinator

Peoria, IL

Full-time

Onsite

Entry, Mid Level

$29.30/hr - $34.47/hr

2+ years exp

OSF HealthCare is dedicated to providing a comprehensive total rewards package for its Mission Partners. They are seeking a Clinical Research Coordinator who will support and coordinate daily clinical research activities, ensuring research is conducted ethically and in compliance with Good Clinical Practices.

Air TransportationEducationElectronic Health Record (EHR)Health CareMedicalTransportation

No H1B

Responsibilities

Support, facilitate and coordinate the daily clinical research activities

Complete most research tasks independently with minimal direction

Assure research is conducted in an ethical manner and all study activities are completed by strictly following Good Clinical Practices (GCP)

Responsible for both clinical and administrative business functions relating to their assigned projects

Play a critical liaison role between study team, department leadership, Institution, Sponsors, and Institutional Review Board (IRB)

Qualification

Certified Clinical Research CoordinatorClinical PracticeClinical research experienceElectronic health recordsMedical terminologyProject Management SkillsAnalytical skillsMicrosoft software proficiencyInterpersonal skillsCommunication skillsProblem solving skills

Required

Bachelor's degree

OR High School Diploma and 4 years of experience in clinical research

Certified Clinical Research Coordinator (CCRC) OR Certified Clinical Research Professional (CCRP)

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

Education: Bachelor Degree 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

Preferred

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

Proficient in medical terminology

Master's Degree in clinical research, healthcare, sciences, business, or related field

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)

Proficient in medical terminology