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Clinical Research Coordinator

  • Clinical Research Coordinator job type Posted on: Nov 06, 2026
  • Clinical Research Coordinator experience level Kelly Science, Engineering, Technology & Telecom
  • Clinical Research Coordinator employment type Gilbert, Arizona
  • Clinical Research Coordinator employment type Onsite
  • Clinical Research Coordinator salary Full-time

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Job Title :

Clinical Research Coordinator

Job Type :

Full-Time

Job Location :

Gilbert Arizona United States

Remote :

No

Jobcon Logo Job Description :

Kelly Science and Clinical FSP is currently seeking a Clinical Research Coordinator (CRC) for one of our established site based partners. This position will be onsite in Gilbert, AZ. The CRC will have overall responsibilities for coordinating efforts with other study team members in order to achieve protocol objectives and corporate goals, including:ESSENTIAL DUTIESDevelop strong working relationships and maintain effective communication with study team members. Develop strong working relationships and become the point of contact for the clinic as well as the sponsor for clinic related activities.Manage multiple concurrent trials Assist with mentoring and training study team members Complete all protocol-related training Perform patient/research participant scheduling Collect patient/research participant history Collects and maintains source documentation Performs data entry and query resolution Collect and review required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, non-clinical supply materials, imaging, and laboratory handling manuals, etc.).

Jobcon Logo Position Details

Posted:

Nov 06, 2026

Reference Number:

10440_4451677699

Employment:

Full-time

City:

Gilbert

Job Origin:

APPCAST_CPC

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Kelly Science and Clinical FSP is currently seeking a Clinical Research Coordinator (CRC) for one of our established site based partners. This position will be onsite in Gilbert, AZ. The CRC will have overall responsibilities for coordinating efforts with other study team members in order to achieve protocol objectives and corporate goals, including:ESSENTIAL DUTIESDevelop strong working relationships and maintain effective communication with study team members. Develop strong working relationships and become the point of contact for the clinic as well as the sponsor for clinic related activities.Manage multiple concurrent trials Assist with mentoring and training study team members Complete all protocol-related training Perform patient/research participant scheduling Collect patient/research participant history Collects and maintains source documentation Performs data entry and query resolution Collect and review required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, non-clinical supply materials, imaging, and laboratory handling manuals, etc.).

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