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Pharmacovigilance comms jobs

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Clinical Nurse Advisor 40574 SLOUGH, BERKSHIRE ...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...
Product Surveillance Reporting Analyst MARLOW, ENGLAND, 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...
GCSP Regions Head of Europe WEST SUSSEX, ENGLAND, UNITED KINGDOM The GCSP Regions Head of Europe is a leadership position for providing end-to-end pharmacovigilance (PV) strategic insight and operational oversight for CSL enterprise affiliates and guiding PV operations in the Affiliates. The role directly manages personnel including Regions Territory Managers...
Looking for Pharmacovigilance Comms 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.
Business Development Director (Pharma/Med-Dev/Consumer) £100 - 125 LONDON ...Regulatory Affairs, Pharmacovigilance, clinical research, and technological solutions. As a trusted collaborator with global life science companies, we are dedicated to excellence and innovation. Your main priority will be selling regulatory affair services into these three sectors of the life...
Global Clinical Safety and PV Regions ODCS (Organized Data Collections Systems) & Digital Media Manager MAIDENHEAD, BERKSHIRE, WINDSOR & MAIDENHEAD, BERKSHIRE; BERKSHIRE; SOUTH EAST ENGLAND; ENGLAND, UK The ODCS (Organized Data Collections Systems) & DM Manager (Digital Media) is a member of the GCSP (Global Clinical Safety and Pharmacovigilance) Regions organization responsible for PV oversight of ODCS, Social and Digital Media programs within the ODCS Hub. This position is responsible for...
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Pharmacovigilance Governance Officer BURTON UPON TRENT, UNITED KINGDOM Pharmacovigilance Governance Officer Ensure that all PV written standards are compliant with corporate and regulatory requirements Further embed a risk-based quality assurance framework which provides evidence that the correct operational processes have been followed in-line with all...
Medical Information Associate (French fluency required) GUILDFORD, ENGLAND, UNITED KINGDOM Company Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially 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...
Medical Information Associate - Dutch Speaking , , UNITED KINGDOM Company Description We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider initially 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...
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 , , 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...
Senior Associate Project Manager (Labelling or Artwork) 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...
Car Fleet Manager HAYES, 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...
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...
Corporate Affairs Associate , , 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 Lead , , 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...
QA Manager & Lead Qualified Person - 3rd Party WOOBURN GREEN, ENGLAND, UNITED KINGDOM ...medical info and pharmacovigilance teams. Main responsibilities: Management of the 3rd party Quality team, ensuring appropriate training plans to ensure their personal development and growth To ensure that batch reviews are completed by the team within the required timeframe for QP...
Technical Support Analyst , , UNITED KINGDOM ...Quality GxP, CMC, Pharmacovigilance, Medical Information / Medical Affairs applications and more. Our mission Our mission is to provide industry-defining implementations that are fast and intuitive to bring our customers an enjoyable and efficient experience. Widely regarded by our customers...
! Validation Engineer (Commissioning) - Globally field based - Global Chemical Manufacturing ! 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...
Global Clinical Safety and PV Regions ODCS (Organized Data Collections Systems) & Digital Media Manager BERKSHIRE, ENGLAND, UNITED KINGDOM The ODCS (Organized Data Collections Systems) & DM Manager (Digital Media) is a member of the GCSP (Global Clinical Safety and Pharmacovigilance) Regions organization responsible for PV oversight of ODCS, Social and Digital Media programs within the ODCS Hub. This position is responsible for...
Lead Clinical Development Scientist (Senior Director), Oncology 81007 ADDLESTONE, SURREY, ADDLESTONE, SURREY ...Knowledge of global pharmacovigilance standards and guidance documents. Comfortable working in a flexible, dynamically changing environment, able to exercise sound judgment, and professionalism with the highest level of scientific integrity. Education/Qualifications: Advanced degree in a...
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