Contract: Full Time.
Salary: Competitive (dependent on experience).
Preparing of internal and external reports relating to signal detection
Supporting safety risk management
Supporting the review of regulatory submission documents
Supporting all regulatory requirements and compliance mandates
BSC in Safety Science, Pharmacovigilance or related field
Knowledge of biostatistical methods used in pharmacovigilance
Experience in drug development is desired
Knowledge of UK & EU safety regulations
Excellent communication skills
I am looking forward to having a chat with you if you are suitable for this role. For more
information on this exciting opportunity please email a copy of your CV in MS WORD format to
email@example.com using Pharmacovigilance Scientist as the Subject.
To stay up to date with the latest and exciting opportunities, please follow us on LinkedIn