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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...
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...
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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...
Key Account & Access Manager - Diabetes
LONDON, GB
...reporting in this area. Pharmacovigilance-Reporting: The Biocon employee should follow and apply within 24h the standard Biocon PV approach if becoming aware about adverse events/side effects and/or incidents including lack of efficacy for Biocon products. Pharmacovigilance department by any of...
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Regulatory & Quality Director
LEATHERHEAD, GB
...guidelines for pharmacovigilance Manage the holding and distribution of our product s regulatory information. Maintain comprehensive knowledge of industry, regulatory, quality, pharmacovigilance and legislative changes and developments. Keep internal processes adherent to UK regulations...
Chief Medical Officer/Chief R&D Officer - Africa Clinical Research Network
OXFORDSHIRE, GB
...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 across the...
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...
QA Manager & Lead Qualified Person - 3rd Party
WOOBURN GREEN, GB
...medical info and pharmacovigilance teams. Main responsibilities: Management of the 3rd party Quality team, ensuring appropriate training plans to ensure their personal development and growth To ensure that batch reviews are completed by the team within the required timeframe for QP...
Automation Project Manager
HATFIELD, 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...
Multiskilled Maintenance Engineer - Global Pharmaceutical Company
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...
Mechanical and Electrical Building Services Technician - Global Pharma
HERTFORDSHIRE, ENGLAND, UNITED KINGDOM
...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...
Cardiac Catheterization Laboratory Nurse
UNITED KINGDOM, , UNITED KINGDOM
...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...
Senior Drug Safety Physician
UNITED KINGDOM, , UNITED KINGDOM
...to our Drug Safety and Pharmacovigilance team, supporting both medically trained and non-medical colleagues. Spearhead training and mentoring initiatives, empowering our team to excel in clinical safety data interpretation and risk management. Act as a subject matter expert in regulatory...
Associate Director, Clinical Safety Scientist
CAMBRIDGE, ENGLAND, UNITED KINGDOM
...clinical safety and pharmacovigilance support to medicines across life cycle. Reporting to the Head of Drug Safety, the Associate Director, Clinical Safety Scientist will lead the clinical safety activities for the assigned compounds within the organization. Responsible for the implementation...
Clinical Scientist
CITY OF LONDON, ENGLAND, UNITED KINGDOM
...trends. Manage pharmacovigilance processes for SAEs and adverse events of special interest (AESI). Work with data management and clinical operations to ensure data entry meets requirements. Oversee any regulatory reporting or actions required. Update Drug Safety Update Report (DSUR) and...
PV Consultant
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
...for: Day-to-day pharmacovigilance oversight : Review SAEs and queries to investigators on a regular basis, support the data cleaning for safety data, and oversee signal management to identify significant trends. Case processing : Manage PVG processes for serious adverse events (SAEs) and...
Automation Project Manager - Global Pharma - Perm
WATFORD, ENGLAND, UNITED KINGDOM
...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...
Senior Research Associate - Protein Sciences
, , UNITED KINGDOM
...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...
Statistical Programmer
, , UNITED KINGDOM
...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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