save this search
Adverts by Google
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...
Senior Pharmacovigilance Manager
WEYBRIDGE
p 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...
Looking for Pharmacovigilance 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.
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...
Qualified Person, Pharmacovigilance (QPPV)
UNITED KINGDOM, UNITED KINGDOM
...maintain the company's Pharmacovigilance system. Being the main point of contact for MHRA competent authority. /p p br /p p Responsibilities: /p ul li Acting as the single point of contact for MHRA competent authority on a 24-hour basis. /li li Ensuring the structure and performance of...
Adverts by Google
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...
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...
Associate Pharmacovigilance Lead
, , UNITED KINGDOM
Associate Pharmacovigilance Lead Alexander Lyons Solutions is excited to partner with a leading client in the pharmaceutical industry to find a talented Associate Pharmacovigilance Lead. This is an exceptional opportunity for a motivated individual to join a dynamic team and contribute to the...
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, Pharmacovigilance Case Processing
UNITED KINGDOM, , UNITED KINGDOM
...quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. Director, Pharmacovigilance (PV) Case Processing...
Senior Safety Physician
UNITED KINGDOM, , UNITED KINGDOM
...extensive knowledge of pharmacovigilance (PV) legislation to contribute to our team. We are looking for an individual who excels in analytical thinking, can navigate complex data, establish structured processes, and effectively communicate information across our global team. Responsibilities...
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...
Quality & Technical Manager
, , UNITED KINGDOM
...holders with respect to pharmacovigilance responsibilities. Report Medical Information and PV data to MA holders Undertake RPi duties for the Company & deputy Consultant RPi as required. Routine Supplier audits with consultant QP/RPi Conduct annual Staff Training for PV & GDP The ideal Technical...
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...
Adverts by Google