Sn. Clinical Pharmacovigilance Scientist
| Dyddiad hysbysebu: | 07 Mai 2025 |
|---|---|
| Cyflog: | £60.0 i £85.0 yr awr |
| Gwybodaeth ychwanegol am y cyflog: | £60 - 85 p/h inside IR35 |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 14 Mai 2025 |
| 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: | 4685017_1746620018 |
Crynodeb
Your new company
My client is a global biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability. They are focused on improving people's quality of life, specialising in neurological diseases.
There is an opportunity for a Senior Clinical Pharmacovigilance Scientist to join their Pharmacovigilance team.
Inside IR35
Hybrid working
Your new role
As a highly motivated individual, you will serve as a product lead for Pharmacovigilance activities within Safety.
The Senior PV Scientist is responsible for overseeing and leading the process for safety signal management activities, aggregate reports (PSURs, DSURs, Line Listings, RMPs), responding to safety questions from internal and external stakeholders, reviewing medical and scientific literature for safety information, and supporting Clinical Trial PV medical activities.
You will serve as a Subject-Matter Expert for Safety and cross-functional teams on relevant global safety regulations and guidelines; data output and analyses; and product-specific information. In this capacity, the Sr. PV Scientist is critical to ensuring products in clinical trials continue to maintain good standing with countries where studies are ongoing to ensure clinical studies are completed, and for marketed products, ensure the marketing authorisation remains in good standing.
What you'll need to succeed
Life sciences degree.
Strong Pharmacovigilance and drug development foundation, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations. Includes knowledge of case processing, expedited reporting rules, and safety database concepts
Leads and conducts, independently and/or collaboratively, all aspects of substantive projects such as signalling, authoring of aggregate data reports, and responses to regulatory agency requests.
Understands, interprets, analyses, and clearly presents scientific and medical data in verbal and written format
Knowledge of common safety database systems.
Demonstrates leadership and interacts collaboratively and effectively in a team environment, as well as with external colleagues
Applies clinical judgment to interpret case information.
Strong organisational skills, including the ability to prioritise independently with minimal supervision.
Excellence in communication
Strong innovation, decision-making and problem-solving skills
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 03330106292
If 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.