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PV Data Associate
GREATER LONDON, GB
...maintain data in the Pharmacovigilance Database. Monitor adverse events received via EEDR. Generate safety data for signal detection and periodic aggregate reports. Supply safety data to the regulatory department for regulatory submissions. Contribute to the continuous enhancement of the...
Multilingual Medical Information Specialist (MMIS) - French
, , 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 Role The Multilingual Medical Information...
Pharmacovigilance Co-ordinator
£35000/annum Excellent Benefits
DARTFORD, KENT, DA1
Our client, based in Dartford, were established in 2011. UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator. Job Description: Develop and approve artwork components and patient information (SPC, PIL, cartons and labelling) and associated mock-ups. Liaise...
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PV Data Associate
GREATER LONDON
...maintain data in the Pharmacovigilance Database. /li li Monitor adverse events received via EEDR. /li li Generate safety data for signal detection and periodic aggregate reports. /li li Supply safety data to the regulatory department for regulatory submissions. /li li Contribute to the...
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...
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Manager, Global Aggregate Reports quality and compliance
TAPLOW, 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...
Pharmacovigilance Auditor
SLOUGH, GB
...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...
Countries and Regions PV Manager
CAMBRIDGE, GB
...delivery of Sobi pharmacovigilance across Sobi countries and regions. Reporting to the Head of Countries & Regions, QPPV and working closely with the Countries & Regions team , the Countries and Regions PV Manager is a key member of the GPV organisation focusing on: The Sobi GPV...
Senior Regulatory Affairs Officer
KENT, GB
...history: 1. Educated to degree level in science or equivalent experience. 2. Proven experience in Regulatory Affairs within the Pharmaceutical industry. 3. Strong communication and project management skills. 4. Proficiency in MS Office suite and regulatory submission portals. Key Words: Regulatory...
Key Account & Access Manager - Diabetes
LONDON, GB
...required: Bachelors degree or higher, ideally in life sciences 5-10+ years pharmaceutical sales experience in the UK Ideally experience in Diabetes and Primary care brands Extensive knowledge of the UK healthcare system and policies Strong working knowledge of newly formed ICS/ICB structure...
Senior Regulatory Affairs & PV Manager
GREATER LONDON, GB
...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...
Product Surveillance Reporting Analyst
MARLOW, GB
...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...
QPPV office and Alliance Management
GREATER LONDON, GB
...You'll Do: Lead global Pharmacovigilance system with finesse, ensuring compliance and efficiency. Dive deep into international agreements, safeguarding Pharmacovigilance standards. Craft and negotiate Drug Safety Agreements, driving global consistency. Seamlessly integrate new products and...
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...
Medical Information Specialist - German Speaking
UNITED KINGDOM, , UNITED KINGDOM
...graduate with a degree in the Life Sciences field, for a Medical Information Specialist position. Main Responsibilities: Manage client requests for medical and safety information from various sources (e.g., phone, email) Provide on-label and off-label information according to regulations...
Decontamination Service Supervisor
ANDOVER, ENGLAND, UNITED KINGDOM
...education, ideally to degree level, or with relevant experience 2 years' experience within a service management position, ideally with a team of direct reports Field service systems experience If you would like to discuss this vacancy further or to discuss your career options in confidence...
Automation Project Manager
HERTFORDSHIRE, ENGLAND, UNITED KINGDOM
...Experience with SQL degree in engineering / computer science / automation Project management certification This is an opportunity to work for a company who is patient focused and research oriented. In this role you'll perform automation Project Management responsibilities for some upcoming...
Regulatory Affairs Associate
MAIDENHEAD, ENGLAND, UNITED KINGDOM
...is essential Bachelor s degree or equivalent in a relevant scientific subject If you would like to discuss this vacancy further or to discuss your career options in confidence, please email me on: tcook-appiah@planet-pharma.co.uk If this role isn t suitable for you, please let us know if you can...
! RBDS Supervisor based in Andover - Leading Chemical manufacturing!
ANDOVER, ENGLAND, UNITED KINGDOM
...requiring a high degree of flexibility and problem solving. Building close working relationships with other territory supervisors, technical experts and equipment specialists will be essential to success in this role. The role is primarily officed based but will occasionally require...
Senior Manager, GCP Quality Assurance
CAMBRIDGE, GB
...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...
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