save this search
Adverts by Google
We've expanded the search to "England" to find more jobs with all your keywords
Pharmacovigilance Systems Product Owner
£50,000
LONDON, SOUTH EAST, UK
Your new company Are you passionate about cutting-edge technology and it's impact on business processes? My client, an established healthcare provider dedicated to providing treatment in Oncology and Rare Diseases across Europe, is looking for a Pharmacovigilance Systems expert to join their team...
Qualified Person, Pharmacovigilance (QPPV)
LUTON, ENGLAND, UNITED KINGDOM
...maintain the company's Pharmacovigilance system. Being the main point of contact for MHRA competent authority. Responsibilities: Acting as the single point of contact for MHRA competent authority on a 24-hour basis. Ensuring the structure and performance of the pharmacovigilance system complies...
PV Physician (Director) - Remote
LONDON, ENGLAND, UNITED KINGDOM
Hobson Prior is currently seeking a PV Physician (Director Level) for a remote position 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...
Looking for Pharmacovigilance jobs in North East?
Top Salaries! Full time, part time and contract.
NORTH EAST
Visit PerfectJobs4U UK for the widest selection of top UK jobs. Full time, part time and work from home roles.
Director, Drug Safety Lead
CAMBRIDGE
...clinical safety and pharmacovigilance support to medicines across life cycle. Reporting to the Head of Drug Safety, this key role will lead the clinical safety activities for the assigned compounds within the organization. br br /p p You will be accountable for the implementation...
Manager, Global Aggregate Reports quality and compliance
BERKSHIRE, ENGLAND, UNITED KINGDOM
...of new and evolving pharmacovigilance legislation within the GRIP process. Coordinates the Aggregate Reports Quality Review Board and overseeing Aggregate report KPIs across CSL business units. The authoring of high quality regulatory required aggregate reports including scientific analysis...
Adverts by Google
Clinical Nurse Advisor
41266
SLOUGH, BERKSHIRE, SL1
...all matters relating to pharmacovigilance, including training requirements and reporting systems. Comply with the relevant regulatory guidelines including the Nursing and Midwifery Council Code, Nursing Midwifery board of Ireland and the Association of British Pharmaceutical Industry Code of...
Senior Medical Director - CNS/Neurology - Europe - Home-based
LONDON, ENGLAND, UNITED KINGDOM
...course of the trial. Pharmacovigilance activity for adverse event analyses and reporting and a medical writing group are integral part of the service offering. Medical Affairs also partner with other functional groups within the Worldwide organization, the generation of statistical and clinical...
Senior Pharmacovigilance Manager
WEYBRIDGE, ENGLAND, UNITED KINGDOM
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 and acting as the UK...
Pharmacovigilance Manager
WINDSOR, ENGLAND, UNITED KINGDOM
Job Title: Quality Manager, Global Quality Management Location: UK (preferably located near Windsor) Are you a Pharmacovigilance professional with a keen eye for quality management? Do you possess experience in audits, inspections, and CAPA management, and aspire to transition into a broader...
Director, Drug Safety Lead
CAMBRIDGE, ENGLAND, UNITED KINGDOM
...clinical safety and pharmacovigilance support to medicines across life cycle. Reporting to the Head of Drug Safety, this key role will lead the clinical safety activities for the assigned compounds within the organization. You will be accountable for the implementation, execution, and...
Regulatory Affairs Manager- Alvita
WOKING, ENGLAND, UNITED KINGDOM
...Regulatory Affairs and Pharmacovigilance in specific projects related to Alvita, including assessing the launch in new territories or the development of new processes necessary to deliver compliance with European and local legislation. You will support the European Head of Pharmacovigilance and...
Automation Engineer
HATFIELD, 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...
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...
Commercial Operations Manager
LONDON AREA, 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...
Computer System Compliance Auditor
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
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 Practice...
Automation Project Manager
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...
Corporate Affairs Associate
CAMBRIDGE, 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...
Automation Engineer
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...
Key Account & Access Manager - Diabetes
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
...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...
Automation Project Manager - Global Pharma - Perm
WATFORD
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of...
Adverts by Google