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Clinical trials coordinator

beBeeSiteManagement
Publicada el 10 diciembre
Descripción

Site management role

at johnson & johnson, we believe health is everything.

* acts as primary local company contact for assigned sites for specific trials.
* may participate in site feasibility and/or pre-trial site assessment visits.
* attends/participates in investigator meetings as needed.

a site manager serves as the primary contact point between the sponsor and the investigational site. A site manager ii is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company standard operating procedures (sop), good clinical practice (gcp), and applicable regulations and guidelines from study start-up through to site closure.



responsibilities

1. primary local contact
2. site feasibility and assessment
3. investigator meetings



key requirements

* clinical trial protocol compliance
* standard operating procedures
* good clinical practice



benefits

this role offers a unique opportunity to contribute to the success of clinical trials and ensure their smooth execution.

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