save this search
Adverts by Google
Pharmacovigilance Auditor
, , UNITED KINGDOM
...audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural science or equivalent number of years...
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...
Pharmacovigilance Auditor
UNITED KINGDOM, UNITED KINGDOM
...audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural science or equivalent number of years...
Looking for Pharmacovigilance Compliance 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.
Associate Director, Pharmacovigilance QA - Home Based / Remote
OXFORD, OXFORDSHIRE, UNITED KINGDOM
...To lead Jazz s Pharmacovigilance QA (GvP) function to assure regulatory compliance and data integrity in all Jazz activities related to Pharmacovigilance. Essential Functions In collaboration with the Sr Dir, Clinical & PV QA, ensures the implementation of the Global Quality strategy, as...
Counsel, PV & Quality, Legal Global Medical Ops
£100 - 125
LONDON
...support in areas of pharmacovigilance and quality assurance (both R&D and PV) for projects of a lower complexity, using a developing, working knowledge of relevant law and the relevant science. The role can work on matters of higher complexity with the direction and supervision of their...
Adverts by Google
Manager, Global Aggregate Reports quality and compliance
MAIDENHEAD, 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. Be one of the first applicants, read the...
Clinical Safety Scientist
£0 - £40 per hour , GBP
BRENTFORD
...Conducting routine pharmacovigilance activities, signal detection/evaluation and leading authoring of key regulatory documents (e.g. DSURs, EU RMPs and PBRERs). Ensuring that all safety documentation is accurate & available to meet global compliance & regulatory requirements. Your Background...
Product Surveillance Reporting Analyst
MARLOW, UNITED KINGDOM
...internal teams such as pharmacovigilance, local in-country teams, and the device quality assurance team to ensure the appropriate and accurate reporting of complaints. Responsibilities: Decision maker for all reportability decisions Lead for all vigilance reporting, including local and global...
Qualified Person, Pharmacovigilance (QPPV)
LUTON, ENGLAND, UNITED KINGDOM
...QPPV to ensure constant compliance with UK PV Legislation and UK Regulations and 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...
Pharmacovigilance Director of Projects (Europe, USA or Canada)
, , UNITED KINGDOM
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...
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...
Quality Specialist
UNITED KINGDOM, , UNITED KINGDOM
...solutions, 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. The Opportunity The Quality...
Senior Drug Safety Physician
UNITED KINGDOM, , UNITED KINGDOM
...studies, ensuring compliance with international safety reporting requirements. Provide invaluable medical expertise to our Drug Safety and Pharmacovigilance team, supporting both medically trained and non-medical colleagues. Spearhead training and mentoring initiatives, empowering our team...
Senior Regulatory Affairs & PV Manager
GREATER LONDON, ENGLAND, UNITED KINGDOM
...maximize regulatory and pharmacovigilance success. knowledge of requirements of MA Transfer in EU territories, which includes requirements of notarization and translations. a team of 4 to ensure day-to-day activities are carried out in Regulatory and Pharmacovigilance. all pre-submission meetings...
QPPV office and Alliance Management
GREATER LONDON, ENGLAND, UNITED KINGDOM
Passionate about transforming lives? Ready to drive innovation in Research & Development? We're on a mission to revolutionise patient care and need your expertise to make it happen. QPPV Office & Alliance Manager (f/m/d) What You'll Do: Lead global Pharmacovigilance system with finesse...
Director, Drug Safety Lead
, , 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
...in place to maintain compliance with the requirements of the Medical Devices Regulation (EU) 2017/745 and the in Vitro Diagnostic Medical Device Regulation (EU) 2017/746, in the context of our obligations as an own brand. You will demonstrate an innovative approach to obtaining market...
Continuous Improvement PMO
, , UNITED KINGDOM
About the company: We are Qinecsa. Trusted partners to global life science companies. We bring together and offer best-in-class pharmacovigilance technology and scientific expertise to connect life science companies to the right safety solutions. Reportum platform Our automated case intake and...
Senior Manager, Quality
ABINGTON PIGOTTS, ENGLAND, UNITED KINGDOM
...programs, ensuring compliance with applicable ICH GCP and GLP standards and global regulations. As an integral member of the team tasked with product development, the position serves as a Quality and compliance business partner, engaging with multiple collaborators. The ideal candidate must...
Global Labelling Lead
UNITED KINGDOM, , UNITED KINGDOM
...Maintain labelling compliance Maintain labelling compliance for assigned products ensuring version control and tracking of CDS implementation in relevant company systems Core labelling supporting documentation Oversee preparation of supporting documents for core labelling changes, in...
Adverts by Google