1 month ago
Hertfordshire Competitive Contract
Job Reference: JG/SPS_1624526877
A top ten pharmaceutical company is seeking an experienced Pharmacovigilance Scientist to join their company on a 6 month contract.
You will be part of their Safety Data Transformation Organisation which processes and reports Individual Case Safety Reports (ICSRs) via the utlisation of current/ future safety systems and co-develops innovative approaches for the transformation and reporting of wider types of safety relevant data, beyond ICSRs.
As Senior Pharmacovigilance Scientist you will be key in transforming and delivering data in order to meet both current and future requirements for a variety of safety related data outputs. As part of your role you will be the Global Processing Business Process Owner and will take ownership and oversight of the case processing process performed. You will provide subject matter expertise into the design and improvement of processes and appropriate documentation which includes the development of metrics, KPIs and business information to support decision making. You will ensure inspection readiness and be the primary point of contact for audits and inspections. Furthermore, you will build strong global networks across the company and maintain an external network.
The successful candidate will be educated to degree level and ideally hold a postgraduate qualification (PhD, PharmD, MD, pharmacovigilance). You will have significant industry experience in areas relevant to pharmacovigilance. You will have excellent knowledge of global pharmacovigilance regulatory obligations and proven ability to lead global line or matrix teams.
Keywords: Pharmacovigilance, Pharmaceutical, Pharm, Contract, Temp, Freelance, Drug Safety, Data Transformation, PV, Drug Safety, pharmacovigilance team manager.