pharmacovigilance physician Work, Jobs in england (with Salaries)

Pharmacovigilance Physician I / II - Fluent in Japanese - 1 year fixed term contract
PrimeVigilance —London
- Remote
- English
- Microsoft Office
- Presentation skills
Quick apply
Associate Director Safety Sciences
BioNTech AG —London
- £146,300 - £234,100 a year
- Full-time
- Doctoral degree
- English
- Communication skills
6d
Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)
サイネオス・ヘルス —London
- Bachelor's degree
- Contracts
- Communication skills
Medical Director, Clinical Development, Hepatology
GlaxoSmithKline —Stevenage
- £202,500 - £371,250 a year
- Full-time
Senior Medical Science Liaison
Merz Aesthetics UK Ltd. —Hemel Hempstead
- Doctoral degree
- Sales
- Microsoft Office
Quick apply
Director, Safety Physician
Summit Therapeutics —Oxford
- £10 - £20 an hour
- Data analysis skills
- Case management
- Computer skills
Quick apply
CRA II / Sr CRA I - FSO - Multi Therapeutics
サイネオス・ヘルス —London
- Bachelor's degree
- Travel
- Contracts
Global Asset Safety Lead
Ipsen Biopharm Ltd —London
- Full-time
- Doctoral degree
- English
- Leadership
Senior Medical Director, Oncology Clinical Development - GU
GlaxoSmithKline —London
- £284,250 - £473,750 a year
- Full-time
- Doctoral degree
- Business development
- Communication skills
- Life insurance
Research Manager - Quantitative Market Research
APLUSA —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- Marketing
- Annual leave
Quick apply

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Associate Director Safety Sciences
BioNTech AG —London
At least 5 years of experience in clinical research with significant exposure to pharmacovigilance activities within biotech/pharmaceutical industries or CROs.
£146,300 - £234,100 a year
6d
Vendor Alliance Lead Associate Director (Cardiac Safety and Respiratory Diagnostics)
Novartis —London
Act as the senior escalation point for vendor issues, driving structured issue resolution and root‑cause analysis.

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Pharmacovigilance Physician I / II - Fluent in Japanese - 1 year fixed term contract

PrimeVigilance -
London

Quick apply

Job details

Fixed term contract

Qualifications

English
Japanese
Microsoft Office
Presentation skills
Communication skills

Full job description

Company Description

We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and becoming one of the global leaders in its fields. We cover all therapy areas including medical devices.

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.

Job Description

For the Client:

To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding, seriousness assessment, Company causality and comment, listedness/expectedness and follow-up questions.
To act as a Qualified Person for Pharmacovigilance or support the Qualified Person for Pharmacovigilance (if not medically qualified) in the medical understanding and evaluation of any safety issues
To review and provide input in Periodic Safety Update Reports, Development Safety Update Reports, literature screening search strategy
To review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety related findings
To cooperate in the preparation of and provide input in Risk Management Plans
Supporting the preparation of responses to regulatory authority requests
Signalling
Reviewing line listings
Participating in signal detection activities including meetings, writing signal detection reports if applicable if required, and providing consultation to clients on aspects related to benefit/risk assessment and risk minimisation
Evaluating and categorizing possible signals and proposing a course of action
Supporting preparation and review of benefit-risk reports

Qualifications

The PV Physician should be medically qualified as a physician
Previous experience in pharmacovigilance
Ability to review different aggregate report types including PBRERs and DSURs
Expertise in signal detection activities is essential
Excellent interpersonal skills
Ability to plan, organise, prioritise and execute multiple tasks
Ability to work effectively cross-culturally and cross-functionally and value the importance of teamwork
Communication skills
Presentation skills
English - advanced (spoken, written)
Japanese - advanced (spoken, written)
Advanced literacy (MS Office)

Additional Information

Why PrimeVigilance

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.

To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.

We offer:

Training and career development opportunities internally
Strong emphasis on personal and professional growth
Friendly, supportive working environment
Opportunity to work with colleagues based all over the world, with English as the company language

Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!

Quality
Integrity & Trust
Drive & Passion
Agility & Responsiveness
Belonging
Collaborative Partnerships

Come and join us in this exciting journey to make a positive impact in patient’s lives. We look forward to welcoming your application.

Quick apply

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pharmacovigilance physician jobs in england

Pharmacovigilance Physician I / II - Fluent in Japanese - 1 year fixed term contract

Associate Director Safety Sciences

Single Sponsor Clinical Trial Manager (previous trial management exp needed (3 days a week in Uxbridge)

Medical Director, Clinical Development, Hepatology

Senior Medical Science Liaison

Director, Safety Physician

CRA II / Sr CRA I - FSO - Multi Therapeutics

Global Asset Safety Lead

Senior Medical Director, Oncology Clinical Development - GU

Research Manager - Quantitative Market Research

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