PV Specialist, US Pharma
Leading US Pharma
Major growth opportunity
About Our Client
Leading US Pharmaceutical Company, globally acknowledged for their innovations in oncology, CNS and rare diseases.
- 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
- 4 years PV experience
What's on Offer
Career opportunities on a truly global scale. Competitive salary and benefit scheme.