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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...
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...
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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...
Senior Implementation Consultant - RIMS (Remote)
£60 - 80
LONDON, REMOTE
...how regulatory information is managed in Life Sciences!Veeva’s Vault RIM suite is the industry’s only unified software solution that provides fully integrated regulatory information management (RIM) capabilities including data and document management, submission publishing and...
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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 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...
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...
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. The Opportunity The Quality Specialist position...
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...
Quality & Technical Manager
, , UNITED KINGDOM
...SOPs Manage Medical Information Service provider & respond to MI enquiries where required. Preparation, management and review of technical agreements and safety data exchange (PV) agreements Liaise with Marketing Authorisation holders with respect to pharmacovigilance responsibilities. Report...
Senior Manager, Quality
ABINGTON PIGOTTS, ENGLAND, UNITED KINGDOM
...Data Management, Pharmacovigilance, etc.) based on analysis and interpretation of applicable regulations. Identify and partner with key collaborator functions and business partners as appropriate. Assist development team business partners with development and documentation of CAPAs 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...
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...
Automation Engineer
HERTFORDSHIRE, ENGLAND, UNITED KINGDOM
...Planet Pharma for more information: oloveland@planet-pharma.co.uk About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested...
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...
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