Pharmacovigilance job, drug safety specialist, biopharma, life sciences, case processing, ICSR
Your new company
Global leading Biopharma
Your new role
Contract role - 12 months initially
Within this role as Drug Safety Specialist, you will be reviewing, preparing, and completing reports of adverse drug experiences, to determine the safety profile of products and to meet regulatory requirements. You will be responsible for data entry, assessment, triage and regulatory reportability and distribution
What you'll need to succeed
Scientific or life science degree.
Experience of Pharmacovigilance activities and processes within the Pharmaceutical Industry, including the Argus, ArisG or equivalent Database.
Previous experience in case processing or a similar role within Pharmacovigilance.
Experience and skill with medical writing is advantageous.
Possess excellent interpersonal, verbal, and written communication skills.
What you'll get in return
Competitive pay rate, 12 month initial contract and possibility of an extension
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.