Are you a business? Hire pharmacovigilance candidates in United Kingdom
The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a Regu...
The GCSP Regions Head of Europe is a leadership position for providing end-to-end pharmacovigilance (PV) strategic insight and operational oversight for CSL enterprise affiliates and guiding PV operations in the Affiliates. The role directly manages personnel including Regions Territory Managers,...
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest ...
The Quality Specialist position supports the delivery of Medical Information and Pharmacovigilance services, to assure ongoing compliance with quality and industry regulatory requirements. The Quality Specialist performs improvement activities through continuous monitoring and evaluation of the q...
CK Group are recruiting for a Clinical Safety Scientist to join a company in the pharmaceutical industry at their site based in Brentford on a contract basis for 12 months. Salary: Up to £40.00 per hour PAYE. This role is inside IR35. Clinical Safety Scientist Role: Assisting with the monito...
At Life Sciences Recruitment Ltd (LSR), we are a Global Life Science recruitment firm that specialises in partnering with start-ups, and fast-growing biotech and pharmaceutical organisations. As one of the most competitive and fast-paced industries globally, succeeding and growing in the life sci...
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ADAMAS is a well-established, leading provider of mission-critical regulatory 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 Practic...
Planet Pharma are currently partnered with a global pharmaceutical manufacturing company who are actively seeking a Automation Project Manager for a permanent position in their UK team. The ideal candidate : experience working within manufacturing and packaging. knowledge of the automation projec...
We are PrimeVigilance (part of Ergomed PLC), a specialized mid-size pharmacovigilance service provider 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...
Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, R&D technology, pharmacovigilance, and medical information services to help solve complex challenges in a dynamic regulatory environment. The Manager, Clinical Trial ...
Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...
Facilitate raising of supplier work orders & purchase orders in line with contract requirements ... Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality ...
Advanced proficiency in MS Office, particularly Excel & PowerPoint; knowledge of TrackWise and ACE is desirable * Excellent written and oral communication skills in English * Strong problem-solving ...
Good Engineering Practices (GEP) are employed in the design, installation and commissioning of ... Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality ...
Continuously monitoring the safety profiles of medicinal products and conducting ongoing safety evaluations throughout the post-authorization period. * Supervising Individual Case Safety Reports ...
Preparing management documentation * Preparation and update of SOPs * Manage Medical Information ... Liaise with Marketing Authorisation holders with respect to pharmacovigilance responsibilities
Extensive experience in clinical safety, pharmacovigilance, and risk management within the pharmaceutical industry * Educated in medicine (MD, MBBS or equivalent) * Good working knowledge of relevant ...
You'd be apart of the Manufacturing IT Team, reporting into the IT Automation Lead. This contract ... Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality ...
... external auditees · Maintain a tracking tool for audits, findings and corrective and preventive actions · Select and manage qualified service providers for Global Quality, e.g., contract auditors ...
The role will be remote 95% of the time, there could be travel into offices based in either ... Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality ...
Must have sterile injectables/Quality Management Systems/Quality Assurance/Medical Information/Pharmacovigilance experience, either from manufacturing generic injectables or pharmaceutical distribution, sterile injectables sales and distribution companies. The upcoming retirement of a long standi...
At Biocon Biologics, we are creating a model for the future of healthcare for all. We are a leading company in the biosimilars revolution where patients come first. Our ambition is to impact a billion lives and we do this by fostering a culture of affordable innovation, patient centricity and dis...
Pharmacovigilance Governance Officer – Pharmaceutical Supplier – Midlands – Up to £29,000 D.O.E The Company Carrot Recruitment are partnered with specialist provider of pharmaceutical products and services who are currently looking for an experience pharmacovigilance professional to join the tea...