Average salary: £72,346 /yearly
More statsSearch Results: 60 vacancies
£41k - £56k per annumEstimated
...pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory...
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£40k - £55k per annumEstimated
...Hobson Prior is seeking a Senior Pharmacovigilance Manager. The successful candidate will maintain the overall safety profiles and any emerging safety concerns concerning the pharmaceutical products. This role is crucial in managing all pharmacovigilance risk management issues...
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£39k - £52k per annumEstimated
...Senior Pharmacovigilance Manager – Biopharmaceuticals - Hertfordshire / Remote
Our client, a global biopharmaceutical company with plants across Europe and North America is looking for a Senior Pharmacovigilance Manager to join their team in the UK.
This is your chance...
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Worldwide
£43k - £58k per annumEstimated
...Join Our Team as a Pharmacovigilance Data Associate in
Introductory Paragraph:
Our client is seeking an experienced and highly-motivated individual to join their team as a Pharmacovigilance (PV) Data Associate. As the PV industry continues to grow at an unprecedented...
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£64k - £87k per annumEstimated
...Site Name: UK - London - Brentford, Belgium-Rixensart, Belgium-Wavre, Warsaw
Posted Date: Feb 20 2024
Pharmacovigilance Scientists - Associate Director/ Director/ Senior Director
Positions in GSK Safety Evaluation and Risk Management (SERM) - Specialty Safety Business...
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Permanent employment
Local area
Immediate start
Flexible hours
£69k - £93k per annumEstimated
...the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating the evolving landscape of international...
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Local area
£44k - £58k per annumEstimated
...talented and dedicated Clinical Safety Scientist to join a global pharmaceutical companiesdynamic team in the UK. They areseeking a Pharmacovigilance Scientist in the Safety Evaluation and Risk Management team within their Global Safety Department, aligned with their HIV...
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£37k - £51k per annumEstimated
...knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We welcome...
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£41k - £56k per annumEstimated
...for our commitment to excellence and service delivery.
We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities...
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£51k - £69k per annumEstimated
...challenges. As part of the team, you will focus on one or more critical areas such as Clinical Development, Regulatory Affairs, Pharmacovigilance/Drug Safety, and Quality Management.
What You'll Do
Lead multiple project engagement teams - empowering the team to plan and...
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Home office
£50k - £60k per annum
...hosting and managing regulatory inspections (GCP/PV)
- Previous work experience in operational functions in clinical development or pharmacovigilance
- Comprehensive understanding of pharmaceutical regulatory requirements and impact on the various functions within the...
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Fixed term contract
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Remote job
£65k - £89k per annumEstimated
...strong communicator and influencing Head, Global Safety Data Integration and Literature to join our leadership team in the Product Pharmacovigilance & Device Safety team, ideally based in our Raleigh (US), Monheim (Germany), Slough (UK) or Brussels (Belgium) offices.
You...
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£41k - £56k per annumEstimated
...specialist knowledge and close relationships with clients and the wider industry make us unique in our field. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal...
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...governance for GPS Safety Sciences deliverables including, but not limited to, Risk Management Plans, Signal Management, and the Pharmacovigilance System Master File.
Establish and refine key performance indicators to ensure overall quality and compliance with associated...
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...care and need your expertise to make it happen.
QPPV Office & Alliance Manager (f/m/d)
What You'll Do:
Lead global Pharmacovigilance system with finesse, ensuring compliance and efficiency.
Dive deep into international agreements, safeguarding Pharmacovigilance...
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Work at office
£42k - £58k per annumEstimated
Hobson Prior is seeking a Senior Pharmacovigilance Manager. The successful candidate will maintain the overall safety profiles and any emerging safety concerns concerning the pharmaceutical products. This role is crucial in managing all pharmacovigilance risk management issues...
Remote job
£122k - £165k per annumEstimated
...drug development and commercialisation:
Patient Insights & Real World Data
Clinical Operations
Quality & Compliance
Pharmacovigilance & Drug Safety
Regulatory Affairs
Market Access
Research & Development Operations
Life Science Policy
Medical Affairs...
£111k - £150k per annumEstimated
...Clinical Professionals) is a specialist division that focuses exclusively on recruitment of Medical Affairs, Clinical Development & Pharmacovigilance for pharmaceutical companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory Authorities.
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Permanent employment
£39k - £53k per annumEstimated
...compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Computer Systems Compliance (CSC) (together...
Remote job
£88k - £119k per annumEstimated
...located in either London or Paris. The successful candidate will be responsible for providing medical and scientific support to pharmacovigilance in accordance with applicable regulatory guidelines/requirements and company Standard Operating Procedures (SOPs).
Maintain close...
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