Clinical Research Coordinator

4 weeks ago

Fort Collins, United States Kelly Science, Engineering, Technology & Telecom Full time

Kelly® Science & Clinical is seeking a Clinical Research Coordinator for a fulltime, contract position with a biotech research site client in Fort Collins, CO. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.


  • No C2C
  • Initial contract is for 3 months but will most likely extend and/or convert to perm.
  • 40 hours per week
  • Onsite in Fort Collins, CO (No relo assisistance)


The Clinical Research Coordinator (CRC I) supports the daily operations of assigned clinical trials. It is the responsibility of the CRC I to communicate with CRC II or CRC III, site manager and study participants regarding necessary information of the study. Adherence to site SOPs is required.


Job Description:

• Inform patients or caregivers about study procedures and outcomes to be expected

• Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional policies

• Have all source documentation filled out and completed while the patient visit is occurring and while the patient is on site for optimal accuracy of data collection

• Have all source documentation completed, entered into EDC within 48 hours of patient visit

• Inventory lab and study supplies. Notify manager when supplies need to be ordered

• Maintain required records of study activity including case report forms, drug dispensation records

• Perform specific protocol procedures such as interviewing subjects, taking vital signs, performing electrocardiograms and taking laboratory specimens

• Record adverse event and side effect data and confer with investigators regarding the reporting of events to sponsors

• Resolve all auto queries in the EDC within 24 hours of query being issued by sponsor

• Dispense medical devices or drugs, and calculate dosages, drug compliance and provide instructions as necessary

• Drug Accountability. Logging new medication shipments and reporting to sponsor received and if lost or damaged. Logging dispensed medication to subjects in appropriate medication log

• Initiate and maintain accurate master logs for each study. (ICF, patient ID, and enrollment).

• Participate in quality assurance audits

• Label and organize space for drug. All drug received should be put in drug cabinets immediately once drug arrives to site after being checked in and logged into the drug logs

• Maintain accurate temperature logs daily as needed

• Other duties as assigned


Required Skills/Abilities:

• 6 months - 2 years clinical research experience preferred

• Ability to work independently and as a member of a team


Education:

• GED or HS Diploma required (Some College preferred)

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