Senior Pharmacovigilance Scientist

ZipRecruiter; London; Remote; GBP 50,000 - 70,000; Full time

Job summary

A leading biopharmaceutical firm is seeking a Senior Pharmacovigilance Scientist to join its team in London. The role involves leading signal management processes and authoring safety reports. Candidates must have a life sciences degree and substantial hands-on experience in Pharmacovigilance. The position offers remote working and requires applicants to reside in the UK. Strong communication, analytical, and leadership skills are essential.

Qualifications

• Several years of hands-on experience in Pharmacovigilance.
• Strong understanding of safety regulations.
• Experience in authoring aggregate safety reports.

Responsibilities

• Lead signal management processes for assigned products.
• Evaluate safety data as part of ongoing pharmacovigilance.
• Author safety sections in aggregate reports.

Skills

Pharmacovigilance

Strong communication

Leadership

Analytical skills

Education

Life sciences degree

Tools

Safety database systems

Job description

Job Description

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 Pharmacovigilance Scientist to join their Pharmacovigilance team.
Inside IR35
Remote working (must be currently living in the UK)

Your new role
As a highly motivated individual, you will serve as a product lead for Pharmacovigilance activities within Safety.
The Senior PV Scientist will lead the signal management process (i.e., signal detection, signal tracking, signal documentation, facilitating decisions regarding signals and safety risk, etc.) for assigned product(s) and evaluate safety data and signals as part of ongoing pharmacovigilance activities. This includes synthesis of data from multiple sources and authoring signal evaluation reports and responding to safety questions from regulatory authorities.You will also lead Aggregate Report management, including strategy, review and finalisation of aggregate safety reports for assigned products, such as PSURs, DSURs, Pharmacovigilance Plans, and Risk Management Plans (RMPs), and authoring safety sections in aggregate reports.

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. With several years of hands-on Pharmacovigilance / Drug safety experience in a pharmaceutical company.
Strong experience in authoring aggregate safety reports, safety signal management 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

Desired Skills and Experience

Pharmacovigilance