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Pharmacovigilance management jobs

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Senior Manager Regulatory Affairs & Pharmacovigilance not provided DARTFORD, KENT, SOUTH EAST, UK Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Senior Manager Regulatory Affairs & Pharmacovigilance. Job Requirements: Define, develop, and leads regional strategies to maximise regulatory and pharmacovigilance success...
Qualified Person for Pharmacovigilance (QPPV - UK) HARROW, GB Qualified Person for Pharmacovigilance (QPPV - UK) Location: Harrow, Middlesex This position is with our sister company Lambda Therapeutic Research Limited The UK QPPV will act in compliance with Regulation (EU) No. 1235/2010 & 520/2012, Directive 2001/83/EC & 2010/84/EU, Applicable...
Global Quality Manager WINDSOR, ENGLAND, UNITED KINGDOM Excellent opportunity to join a leading pharma company as a Senior Manager - Global Quality Management. The main task is to manage and perform audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the inspection management, the...
Looking for Pharmacovigilance Management jobs? Top Salaries! Full time, part time and contract. Visit PerfectJobs4U UK for the widest selection of top UK jobs. Full time, part time and work from home roles.
Qualified Person for Pharmacovigilance (QPPV - UK) p strong Qualified Person for Pharmacovigilance (QPPV - UK) /strong /p p strong Location: Harrow, Middlesex /strong /p p br br Remember to check your CV before applying Also, ensure you read through all the requirements related to this role. br /p p strong This position is with our...
Pharmacovigilance Co-ordinator (Permanent) DARTFORD, KENT, KENT; SOUTH EAST ENGLAND; ENGLAND, UK Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator. Job Description: Develop and approve artwork components and patient information (SPC, PIL, cartons and labelling) and associated mock-ups. Liaise...
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Manager Auditor SANDWICH, KENT, UNITED KINGDOM ...GCP, Regulatory and Pharmacovigilance regulations and guidelines as well as Pfizer policies and procedures Independently conducts/leads more complex routine audits for at least one vendor type (e.g. study conduct, pharmacovigilance service providers), supports non-routine and vendor oversight...
Qualified Person for Pharmacovigilance (QPPV - UK) UNITED KINGDOM, UNITED KINGDOM p b Qualified Person for Pharmacovigilance (QPPV - UK) /b /p p b Location: Harrow, Middlesex /b /p p br /p p b This position is with our sister company Lambda Therapeutic Research Limited /b /p p br /p p The UK QPPV will act in compliance with Regulation (EU) No. 1235/2010...
Pharmacovigilance Co-ordinator £35000/annum Excellent Benefits DARTFORD, KENT, DA1 Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator. Job Description: Develop and approve artwork components and patient information (SPC, PIL, cartons and labelling) and associated mock-ups. Liaise...
Manager, Pharmacovigilance and Medical Information - FTC LONDON, UNITED KINGDOM JOB DESCRIPTION To be considered for an interview, please make sure your application is full in line with the job specs as found below. Job title: Manager, Pharmacovigilance and Medical Information - FTC Reporting to: Director, Scientific Affairs Department: Scientific Affairs CNX Therapeutics is a...
Manager, Pharmacovigilance and Medical Information - FTC LONDON, GB JOB DESCRIPTION Job title: Manager, Pharmacovigilance and Medical Information - FTC Reporting to: Director, Scientific Affairs Department: Scientific Affairs CNX Therapeutics is a European pharmaceutical company dedicated to improving the lives of patients through the supply of essential medicines...
Manager, Drug Safety CAMBRIDGE, GB ...clinical safety and pharmacovigilance support to medicines across life-cycle. Reporting to the Head of Drug Safety, you will oversee the drug safety operation and compliance activities for the development programmes and ensuring inspection readiness. Key responsibilities: Serve as the main...
Automation Project Manager HATFIELD, GB ...strategy. Management of the specification, design, development, and handover of automation systems in a secure and compliant manner Generation of project management documentation approved at appropriate gate reviews including: Proposal Charter Execution Plan (PEP) Report Responsible...
Countries and Regions PV Manager CAMBRIDGE, GB ...delivery of Sobi pharmacovigilance across Sobi countries and regions. Reporting to the Head of Countries & Regions, QPPV and working closely with the Countries & Regions team , the Countries and Regions PV Manager is a key member of the GPV organisation focusing on: The Sobi GPV...
Regulatory & Quality Director LEATHERHEAD, GB ...relations, issue management, corporate and social responsibility, strategic communications, and information distribution. The Regulatory & Quality Director is the named person on all external regulatory licenses and external pharmaceutical, regulatory and government bodies. Core...
Key Account & Access Manager - Diabetes LONDON, GB ...strategies: Area Management: Effective management of the territory through the optimal selection of activities for the management of healthcare institutions, doctors, pharmacists, and medical staff considering the knowledge of the decision-making areas visited persons or prescribing...
Chief Medical Officer/Chief R&D Officer - Africa Clinical Research Network OXFORDSHIRE, GB ...biostatistics, data management, pharmacovigilance and beyond Craft a bold research agenda that addresses Africa's most pressing health needs, with a focus on delivering affordable, accessible and scalable innovations Build and oversee a portfolio of sponsored and investigator-initiated trials...
QA Manager & Lead Qualified Person - 3rd Party WOOBURN GREEN, GB ...be responsible for the management of all Quality aspects involving our CMO business, ensuring compliance with the 3rd party QMS. You will resolve day-to-day issues to maintain the quality of supply as well as providing technical input into projects such as product transfers. You will be the...
Senior Director, Medical Affairs & Clinical Development LONDON, GB ...regulatory affairs, and pharmacovigilance processes. Demonstrated track record of successful product launches and lifecycle management strategies. Excellent communication and presentation skills, with the ability to effectively engage with internal and external stakeholders. Proven leadership...
! Building Services Technician - Onsite - Leading Pharmaceutical! SAINT ALBANS, GB ...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their...
Key Account Manager LUTON, GB ...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their...
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