Average salary: £60,780 /yearly
More stats ...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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Date Added: Tue 26/03/2024
Manager, Pharmacovigilance & Epidemiology (PVE)
7 - 10)+ years industry experience as an epidemiologist/observational research scientist
* Virology RWE/RWD experience...
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...learn and develop new Regulatory skills.
Liaise closely with Business Development (where required), Regulatory Science, Pharmacovigilance, Product Launch, Artwork, Supply Chain and Quality colleagues to ensure alignment in all initiatives.
Prepare...
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Hybrid work
Flexible hours
...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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...They are looking for a QPPV to ensure constant compliance with UK PV Legislation and UK Regulations and maintain the company's Pharmacovigilance system. Being the main point of contact for MHRA competent authority.
Responsibilities:
Acting as the single point of contact...
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Temporary work
...Process - ensuring quality whilst taking time and cost out of drug development
Reporting to the Vice President and Head of Pharmacovigilance and Drug Safety Services, the Director Drug Safety, Europe will play a key role in the continued growth, direction, leadership and...
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Permanent employment
Relocation package
Flexible hours
...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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Permanent employment
Local area
...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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Permanent employment
Full time
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For contractors
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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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Contract work
£39k - £51k per annumEstimated
...relationship building, and partnership.
Actively participating in and supporting required QMS activities, including complaint and pharmacovigilance reporting.
Your Background
Degree qualified in life science or equivalent....
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Permanent employment
Night shift
3 days week
...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...
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Remote job
...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
...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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Remote job
...regulations and to ensure inspection readiness.
Participate in Audit and Inspection planning with Clinical Development Quality and Pharmacovigilance Quality Assurance.
Attend improvement initiatives to improve quality and compliance processes and effectiveness in...
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Local area
...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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...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...
Work from home
Home office
...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...
Work at office
...regulations and to ensure inspection readiness.
Participate in Audit and Inspection planning with Clinical Development Quality and Pharmacovigilance Quality Assurance.
Represent or ensure GCSO representation and preparation during audits/inspections (on-site by internal and...
Contract work
Local area
...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.
#
Permanent employment
...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.
#
Permanent employment
Hybrid work
...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...
Permanent employment
For contractors
Work at office
...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 are an equal...
Permanent employment
For contractors
Work at 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...
Contract work
Fixed term contract
Work at office
Remote job
...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...
Permanent employment
For contractors
Work at office
...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.
#
Permanent employment
...Central London, we operate compliantly in 30+ countries with a network of 2500+ active contractors globally. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal...
For contractors
Work at office
...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.
#
Permanent employment
Worldwide
...areas and with a variety of functional stakeholders, including marketing, scientific engagement, supply chain, finance, medical, pharmacovigilance, manufacturing, quality, procurement, engineering, contracting, communications, and business development.
Intense sense of...
Permanent employment
Contract work
Private practice
Local area
Work from home
...validation / GxP in regulatory environment and knowledge of key governing regulations such as 21 CFR Part 11. Experience in working with Pharmacovigilance data structures and standards, i.e. E2B, MedDRA, WHO Drug. Experience in working with major Signal Case Processing systems, e.g....
...recruitment, coaching, and performance management.
Oversee and manage all relevant internal systems, ensuring compliance with Pharmacovigilance, CRM systems, expenses systems, and PM systems.
Develop and nurture customer relationships to enhance therapy area knowledge...