Job Overview
Employment Type
Hourly
Full-time
Compensation
Type:
Hourly
Rate:
Range $36.00 - $49.00
Work Schedule
Standard Hours
Benefits
Health Insurance
Dental Insurance
Paid Time Off
401(k) retirement plan
Professional development opportunities
Employee wellness programs
Vision Insurance
Job Description
CommonSpirit Health is a leading nonprofit Catholic healthcare system committed to delivering integrated health services and improving health outcomes across the United States. Inspired by faith, driven by innovation, and powered by humankindness, CommonSpirit Health provides care through more than 2,300 clinics, care sites, and 137 hospital-based locations, complemented by home-based services and virtual care offerings. With over 157,000 employees, including 45,000 nurses and 25,000 physicians and advanced practice providers, the system delivers more than 20 million patient encounters annually. CommonSpirit Health is also distinguished by its commitment to community, contributing over $4.2 billion annually in charity care, community benefits,... Show More
Job Requirements
- Bachelor's degree in a science or related field or equivalent experience
- at least 3 years of clinical trial coordination experience
- experience with at least 5 drug or device trials as primary coordinator
- 3 years of healthcare patient interaction experience
- proficiency with electronic data capture software
- familiarity with Clinical Trial Management Systems
- willingness to obtain CCRP or CCRC certification within 12 months
- Certified Phlebotomy Technician (ANCC) certification preferred
- adherence to federal and state research regulations and CommonSpirit Health policies
Job Qualifications
- Bachelor's degree in a science or related field or equivalent combination of education and job-related experience
- minimum of 3 years experience conducting clinical trials
- experience as primary research coordinator for at least 5 drug or device trials
- 3 years of patient interaction experience in healthcare settings
- proficiency with electronic data capture software and Clinical Trial Management Systems
- certification as Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator via ACRP or SCRA within 12 months
- Certified Phlebotomy Technician (ANCC) certification is a plus
Job Duties
- Coordinate and participate in site initiation and sponsor-required training for protocols
- dispense study medication to research participants under the direction of the Principal Investigator or coordinate with hospital pharmacy staff
- process clinical trial labs including specimen collection, centrifuging, aliquoting, and shipping in compliance with federal regulations
- conduct informed consent processes, document discussions, and obtain required signatures
- coordinate all study-required visits, procedures, tests, and activities and schedule participant appointments
- perform timely and accurate data collection and reporting according to protocol, sponsor requirements, and regulations
- identify and report adverse events and protocol deviations to sponsors and IRBs
- serve as liaison among participants, investigators, sponsors, IRBs, administration, patient care coordinators, and insurance to support protocol interpretation and clinical questions
- collaborate with billing staff to ensure clinical trials are performed per organizational requirements and complete Research Encounter Forms for participant visits
Job Qualifications
Experience
Mid Level (3-7 years)
Job Location
We didn't receive the exact location for this job posting,
please contact the employer.
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