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PV Data Associate
GREATER LONDON, GB
...team in managing safety data, including adverse events, in line with regulatory standards and company SOPs. Process cases and perform MedDRA coding of safety events as per the latest version. Enter and maintain data in the Pharmacovigilance Database. Monitor adverse events received via EEDR...
Data Protection Manager - Global Manufacturing Pharma
HERTFORDSHIRE, ENGLAND, UNITED KINGDOM
Title: Data Protection Manager - Global Manufacturing Pharma Type: 12-month FTC Location: Hertfordshire We've partnered with a global manufacturing Pharma company who are looking for a Data protection Manger to manage AI impact assessment framework to ensure compliance with relevant AI, data...
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
...team in managing safety data, including adverse events, in line with regulatory standards and company SOPs. /li li Process cases and perform MedDRA coding of safety events as per the latest version. /li li Enter and maintain data in the Pharmacovigilance Database. /li li Monitor adverse events...
Data Protection Manager - Global Manufacturing Pharma
UNITED KINGDOM, UNITED KINGDOM
p Title: Data Protection Manager - Global Manufacturing Pharma /p p Type: 12-month FTC /p p Location: Hertfordshire /p p br /p p We've partnered with a global manufacturing Pharma company who are looking for a Data protection Manger to manage AI impact assessment framework to ensure...
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Manager, Global Aggregate Reports quality and compliance
MAIDENHEAD, SOUTH EAST, 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...
Key Account & Access Manager - Diabetes
LONDON, GB
...Reporting & Data base update, & Sales Analysis Reliable and timely planning and reporting activities and results, updating database in accordance with the company requirements. Observation and analysis of competitors' actions and reporting in this area. Pharmacovigilance-Reporting...
Senior Drug Safety Physician
UNITED KINGDOM, , UNITED KINGDOM
...to our Drug Safety and Pharmacovigilance team, supporting both medically trained and non-medical colleagues. Spearhead training and mentoring initiatives, empowering our team to excel in clinical safety data interpretation and risk management. Act as a subject matter expert in regulatory...
Continuous Improvement PMO
UNITED KINGDOM, , 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...
Regulatory Affairs Manager- Alvita
WOKING, ENGLAND, 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...
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...
Senior Research Associate - Protein Sciences
, , UNITED KINGDOM
...to interpret complex data. player with the ability to work in cross-functional teams with different skills. Responsibilities : Development and delivery of analytical methods for characterisation with a key focus on analytical method development for mAb, mAb2 and mRNA delivery, UPLC (SEC, HIC...
Senior Manager, GCP Quality Assurance
CAMBRIDGE, GB
...Clinical Operations, 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...
Senior Business System Analyst - Development
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
...create the Development data and IT solution landscape and roadmap Partner with internal and external stakeholders and driving innovation Ensure that all IT products are compliant with internal security, risk management policies and practices, external regulatory and statutory requirements...
Human Resources Operations Manager
UNITED KINGDOM, , UNITED KINGDOM
...of people processes and data across Europe and New Markets. You will support the HR team by participating in the design and management of the workflows supporting Talent Acquisition, Talent Management, Total Rewards, and HR Business Partner activities, as well as partnering with teams such as IT...
Global Labelling Lead
UNITED KINGDOM, , UNITED KINGDOM
...the Company Core Data Sheet (CDS), Global Patient Leaflet and Target Label Profile Maintain labelling compliance Maintain labelling compliance for assigned products ensuring version control and tracking of CDS implementation in relevant company systems Core labelling supporting...
Market Research & Insights
LONDON, GB
...commercial and medical data, and primary market research methods and applications Successful track record in previous market research and project management roles within the pharmaceutical industry (agency or client side) for at least 5 years Knowledge of pharmaceutical industry is a must and...
IT Manufacturing Project Manager
WEST MIDLANDS, GB
...2024. Requirements: Data Integrity Knowledge Pharmaceutical Industry Experience (GxP) BMS, EMS and SCADA Systems Experience and Knowledge Knowledge of IT and OT areas Ability to understand complex application and OT asset landscape If you would like to discuss this vacancy further or to...
Quality Specialist - Medical Information
, , 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...
Change Management Specialist
UNITED KINGDOM, , 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...
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