Job Description
Description
Overview
As a Site Activation Partner, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
Le partenaire d’activation du centre de l’étude est chargé de soutenir les activités opérationnelles liées à l’évaluation, l’activation, l’initiation, la surveillance et la clôture des centres/études des chercheurs assignés, afin de garantir le respect des délais de l’étude et conformément aux lois, aux bonnes pratiques cliniques et aux normes en vigueur.
Vous fournirez un soutien technique et logistique aux SRP pour assurer l’initiation des chercheurs et le démarrage de l’étude.
Responsibilities
What you will be doing:
Clinical Trial Site Activation & Conduct
- Assist with study site activation activities to ensure timely site activation.
- Register investigator sites in registries as required.
- Support and/or coordinate central Investigator Review Board (IRB) submissions when needed.
- Work with investigator sites to complete critical information for site activation, including Investigator Initiation Packages (IIP), confidentiality agreements, study contracts, clinical supply shipment information,
Company
Pharmaceutical Research Associates, Inc
Location
, , Canada
Country
Canada
Salary
150.000
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