Job Description
**1. Job title:**
As a **Clinical Study Manager CT** , you will be responsible for the execution and regulatory compliance of clinical studies for CT
**2. Your role:**
* Participates in the handling of clinical studies, in compliance to all applicable regulations (like ISO, GCP and FDA) and Philips procedures, working under limited supervision.
* Ensures strict adherence to study protocols, regulatory standards, and Philips Processes/Procedures through meticulous execution of site assessment, on site and remote monitoring and training, and close-out visits, proactively addressing deviations and ensuring data accuracy and study integrity.
* Works with study sites and investigators to provide support and guidance on protocol requirements, study procedures, and regulatory expectations.
* Acts as a subject matter expert to provide guidance on GCP, ISO and FDA regulatory requirements for the conduct of research involving human subjects i...
As a **Clinical Study Manager CT** , you will be responsible for the execution and regulatory compliance of clinical studies for CT
**2. Your role:**
* Participates in the handling of clinical studies, in compliance to all applicable regulations (like ISO, GCP and FDA) and Philips procedures, working under limited supervision.
* Ensures strict adherence to study protocols, regulatory standards, and Philips Processes/Procedures through meticulous execution of site assessment, on site and remote monitoring and training, and close-out visits, proactively addressing deviations and ensuring data accuracy and study integrity.
* Works with study sites and investigators to provide support and guidance on protocol requirements, study procedures, and regulatory expectations.
* Acts as a subject matter expert to provide guidance on GCP, ISO and FDA regulatory requirements for the conduct of research involving human subjects i...
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