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Experienced Clinical Research Associate, Multi-Sponsor, France

Company

IQVIA

Location

Illkirch-Graffenstaden, France

Type

Full time

Job Description

Job Overview


Conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.

Essential Functions

  • Complete appropriate therapeutic, protocol and clinical research training to perform job duties.

  • Work with experienced clinical staff.

  • Perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.

  • Administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.

  • Ensure the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage ...

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