save this search
Adverts by Google
Pharmacovigilance Scientist x2
£35,000 - £40,000 per annum
STRATFORD, LONDON
p 4,000 professionals, 0 days wasted, 1 incredible purpose. Together, we are beating cancer. /p br br Make sure to apply with all the requested information, as laid out in the job overview below. br br p strong Pharmacovigilance Scientist x 2 - Centre for Drug Development /strong /p br br...
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 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...
Looking for Pharmacovigilance Information 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.
Clinical Nurse Advisor
41266
SLOUGH, BERKSHIRE, SL1
...to activity reporting, information feedback and expenses Quality and Compliance Undertake Client and Inizio Engage training to include: Programme specific training Mandatory training incl. Safeguarding Level 3, BLS, anaphylaxis. Product Quality Complaint (adverse event and product...
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
Consumer Safety Coordinator
WEYBRIDGE, ENGLAND, UNITED KINGDOM
About the role The Consumer Safety coordinator is a position responsible for the collection and maintenance of key safety information to support the efficient and compliant functioning of the consumer safety function. Key responsibilities Supporting the collection/coordination of safety data to...
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
GREATER LONDON, ENGLAND, UNITED KINGDOM
Job title: Medical information & PV Manager A Pharmaceutical business in London is looking for a Medical Information and Safety Manager to join their team. This role ensures the Quality, consistency and effective management of Medical Information and Pharmacovigilance systems and enquiries...
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...
Multilingual Medical Information Specialist - Norwegian Speaking
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. The Multilingual Medical Information Specialist...
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 Quality Specialist
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. Position overview The Senior Quality Specialist...
Regulatory Affairs Manager- Alvita
WOKING, ENGLAND, UNITED KINGDOM
...respond to requests for information from national competent authorities. You will be responsible for becoming the subject matter expert on medical devices within the business and ensuring plans are in place to maintain compliance with the requirements of the Medical Devices Regulation (EU...
Global Product Safety Scientist
CAMBRIDGE, ENGLAND, UNITED KINGDOM
...key role within Global Pharmacovigilance & Patient Safety (GPV) and is responsible for providing scientific expertise to safety surveillance and risk management activities including signal detection and evaluation for assigned product(s), where Sobi is the marketing authorisation holder or has...
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...
Complaints Intake Analyst
, , UNITED KINGDOM
...activities for missing information, coordinating the logistics of complaint sample returns and communicating the results of the complaint investigations when requested/required. Communication and cooperation with customers and distributors involved in the reported complaints Internal...
Technical Support Analyst
UNITED KINGDOM, , UNITED KINGDOM
...Content and Regulatory Information Management technology for regulated industries globally. ISO 27001 accredited, eight of the top 10 global life sciences companies rely on Generis flagship Intelligent Content Services platform, CARA for critical document and information management, including...
Senior Product Lifecycle Management Consultant - Biologics
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. Job Description This Senior Consultant Product...
Director of Regulatory Affairs
UNITED KINGDOM, , UNITED KINGDOM
...R&D technology, pharmacovigilance, and medical information services to help solve complex challenges in a dynamic regulatory environment. With our mission to improve the health and safety of patients, we are focused on delivering the highest quality of services throughout the full product...
Regulatory Clinical Trials Submission Manager
UNITED KINGDOM, , UNITED KINGDOM
...R&D technology, pharmacovigilance, and medical information services to help solve complex challenges in a dynamic regulatory environment. With our mission to improve the health and safety of patients, we are focused on delivering the highest quality of services throughout the full product...
Adverts by Google