CLINICAL RESEARCH COORDINATOR

Kelly Services

OK, United States

Temporary

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Job details

Kelly Science & Clinical® is seeking a Contract Clinical Research Coordinator for a Short-Term Contract 4-6 month effort that will be fast moving.

Excellent opportunity for individuals experienced in multiple studies simultaneously and within a dynamic work environment.

Position : Clinical Research Coordinator I Short-Term Contract

Location : Yukon OK and Edmond OK

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.

Reports to : Site Manager / Director

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
GED or HS Diploma required (Some College preferred)
Ability to work independently and as a member of a team

Education and Experience :

College or medical certification required

Physical Requirements :

Prolonged periods of sitting at a desk and working on a computer
Must be able to lift up to 15 pounds

If You Qualify - APPLY TODAY!

9511701

1 day ago

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