Manager, Drug Safety
Top3 global CRO
About Our Client
Global CRO, leading in Asia-Pacific region and Japan with in-house diagnostic lab.
- Contributes to the development and/or review of Clinical Trial Protocols, Case Report Forms and Adverse Event Reporting forms.
- Consistently responsible for assisting with the set-up of, and the provision of data to, Safety Committees / Drug Safety Monitoring Boards.
- Assist in the co-ordination of endpoint committees.
The Successful Applicant
- line management and/or project management experience.
- relevant to pharmacovigilance/drug safety knowledge
What's on Offer
Development of a growing business unit directly under APAC. Career opportunities on a truly global scale.