- The DrugSafetyAssociate will provide technical and process-related support to drugsafety
management (clinical trial and post-marketed) and medical monitoring
activities, regulatory information collection and organization,
ensuring compliance with relevant regulations and Standard Operating
Procedures (SOPs).
For members of the Global Pharmacovigilance Information Office (GPIO):
o Support collection and organization of global PV requirements
o Data entry and maintenance of country specific requirements in PAREXEL PV repository
o Receipt and triage of requests for updates to country requirements
o Communicate country-specific regulatory updates to project teams as required
o Maintain updated network list of Named Safety Contacts/LQPPV
o Work directly with relevant stakeholders on standalone GPIO projects
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