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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...
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...
Countries and Regions PV Manager
CAMBRIDGE
...delivery of Sobi pharmacovigilance across Sobi countries and regions. br /p p 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: /p ul...
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Qualified Person for Pharmacovigilance (QPPV - UK)
UNITED KINGDOM, UNITED KINGDOM
p b Qualified Person for Pharmacovigilance (QPPV - UK) /b /p p b Location: Harrow, Middlesex /b /p p br /p p b This position is with our sister company Lambda Therapeutic Research Limited /b /p p br /p p The UK QPPV will act in compliance with Regulation (EU) No. 1235/2010...
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...
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! Marketing Manager - Hybrid in Andover - Leading Chemical manufacturing!
ANDOVER, GB
...looking for minimum BSc degree and 5 years of professional experience or MBA in Marketing with 3 years of experience (Scientific degree advantageous) Business-to-business marketing experience in Life Science industries Experience in successfully marketing and selling complex high-value capital...
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...
Freelance/Contract Validation Microbiologist
HAMPSHIRE, GB
...amp; 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 ProPharma is currently...
Automation Project Manager
HERTFORDSHIRE, GB
...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...
Clinical Education Manager - Medical Device
CROYDON, GB
...including complaint and pharmacovigilance reporting. Job Requirements: Education and Experience: Registered Nurse qualification. Minimum 24 months of experience in Intensive Therapy Unit (ITU). Proficiency in Continuous Renal Replacement Therapy (CRRT). Experience in teaching and supporting in...
Automation Project Manager - Global Pharma - Perm
WATFORD, GB
...databases / Historians Degree (or HNC/HND) qualification in engineering, computer science, automation, or related engineering discipline EngTech / IEng / CEng or working towards professional status Professional membership (i.e. BCS, IET, ISPE) Project management certification (i.e. CAPM / PMP) If...
Regional Co-Ordinator
WEST MIDLANDS, GB
...Bachelor's degree in a relevant field (e.g., life sciences, business administration). Previous experience in pharmaceutical or healthcare industry, preferably in a similar coordination or project management role. Strong understanding of compliance regulations governing interactions...
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...
Clinical Trial Project Manager
, , UNITED KINGDOM
...finance, medical and pharmacovigilance). Proactively communicates with the sponsor and internal groups ensuring that they have all the information required on project progress and status (risk analyses, what-if scenarios, contingency plans, technical information, significant changes of any...
Regional Coordinator
, , UNITED KINGDOM
...Bachelor's degree in a relevant field (e.g., life sciences, business administration). Previous experience in pharmaceutical or healthcare industry, preferably in a similar coordination or project management role. Strong understanding of compliance regulations governing interactions...
Freelance CRA - Experienced
UNITED KINGDOM, , UNITED KINGDOM
...medical writing, pharmacovigilance, biostatistics, project management, and medical communication services. Whether you are a freelance consultant or a company in need of support, Pharmalancers simplifies the process of connecting and finding the right fit. Role Description This is a...
Regional Coordinator
, , UNITED KINGDOM
...Bachelor's degree in a relevant field (e.g., life sciences, business administration). Previous experience in pharmaceutical or healthcare industry, preferably in a similar coordination or project management role. Strong understanding of compliance regulations governing interactions...
Qualified Person for Pharmacovigilance (QPPV - UK)
, , UNITED KINGDOM
Qualified Person for Pharmacovigilance (QPPV - UK) Location: Harrow, Middlesex This position is with our sister company Lambda Therapeutic Research Limited The UK QPPV will act in compliance with Regulation (EU) No. 1235/2010 & 520/2012, Directive 2001/83/EC & 2010/84/EU, Applicable National Laws...
Senior Director, Medical Affairs & Clinical Development
, , UNITED KINGDOM
...Requirements: Medical degree required with GMC registration. Experience in medical affairs leadership roles within the pharmaceutical industry. Strong understanding of clinical development, regulatory affairs, and pharmacovigilance processes. Demonstrated track record of successful product...
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...
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