Pharmacovigilance Scientist - Outsourcing Oversight manager
| Dyddiad hysbysebu: | 05 Mehefin 2024 |
|---|---|
| Cyflog: | £40.0 i £50 yr awr |
| Gwybodaeth ychwanegol am y cyflog: | Hourly Rate |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 12 Mehefin 2024 |
| Lleoliad: | Maidenhead, Berkshire, SL6 3UD |
| Gweithio o bell: | Hybrid - gweithio o bell hyd at 3 ddiwrnod yr wythnos |
| Cwmni: | Hays Specialist Recruitment |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | 4571399_1717600895 |
Crynodeb
Your new company
My client, a global pharmaceutical and biotech company with a goal of contributing to healthcare innovation and environmental sustainability. They are focused on improving people's quality of life by preventing, alleviating, and curing diseases. They have a wide pharmaceutical portfolio, specialising in some of the following areas: Oncology, neuroscience, and rare diseases. There is an opportunity for a Pharmacovigilance Scientist, Outsourcing Oversight Manager to join their Vendor Management team on a 12-month rolling contract.
Inside IR35Onsite 2/3 days per week
Your new role
As a highly motivated individual, you will join their Vendor Management team as a Pharmacovigilance Scientist, Outsourcing Oversight Manager, where you will be responsible for the outsourced activities within the Safety Surveillance and Aggregate Report (SSA) group. These outsourced activities may include the planning and production of aggregate reports, risk management plans and signal detection services. The Outsourcing Oversight Manager, PV Scientists, will support with oversight over multiple vendors and the daily vendor activities and support where needed with SSA process improvements.
What you'll need to succeed
You will hold a bachelor's degree in biologic or natural science, or health care discipline. Advanced degree (PhD, MPH, NP, PharmD, etc.) is preferred.You will be familiar with Pharmacovigilance and drug development, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations. Includes familiarity with case processing, expedited reporting rules, and safety database concepts.You will possess great knowledge of aspects of aggregate reports, signal detection processes and/or risk management plans. Excellent knowledge or experience of aspects of outsourcing and/or vendor oversight. Be able to understand, interpret, analyse, and clearly present scientific and medical data in verbal and written format Strong skills in performing editorial, technical, and scientific authoring.Interact collaboratively and effectively in a team environment.Strong communication and organisational skills, including the ability to prioritise independently.Knowledge of common data processing software (SharePoint, EXCEL, PowerPoint, Microsoft Word, Business Objects). Knowledge of common safety database systems, i.e. Argus and ArisG
What you need to do now
Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and residing in the UK.If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.