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Associate Director, Pharmacovigilance QA - Home Based / Remote
OXFORD, ENGLAND, GB
...early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees...
Pharmacovigilance Auditor
, , 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...
PV Physician (Director) - Remote
LONDON, ENGLAND, UNITED KINGDOM
Hobson Prior is currently seeking a PV Physician (Director Level) for a remote position located in either London or Paris. The successful candidate will be responsible for providing medical and scientific support to pharmacovigilance in accordance with applicable regulatory guidelines/requirements...
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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...
Medical Director – Medical Affairs & Clinical Dev
£200 +
LONDON
...Affairs and Clinical Development /p br p Location: London /p br p Salary: Competitive /p br p Benefits: bonus, pension, healthcare /p br p JO-2307-518982 /p br p A unique opportunity has arisen for a Medical Affairs Physician to expand their leadership capabilities, leading on not...
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Clinical Safety Scientist
£0 - £40 per hour , GBP
BRENTFORD
...Conducting routine pharmacovigilance activities, signal detection/evaluation and leading authoring of key regulatory documents (e.g. DSURs, EU RMPs and PBRERs). Ensuring that all safety documentation is accurate & available to meet global compliance & regulatory requirements. Your Background...
Senior Administrative Assistant - R&D
OXFORD, ENGLAND, GB
...early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees...
Senior Manager Pharmacology, Neuroscience (Remote)
OXFORD, UNITED KINGDOM
...early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees...
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...
Senior Business System Analyst - Development
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
Role: Senior Business System Analyst - Development Location: United Kingdom - Remote Salary: Very competitive salary on offer Planet Pharma are supporting a leading global pharma company with the search for a new Senior Business System Analyst - Development to join them during an exciting period of...
Regulatory Affairs Manager- Alvita
WOKING, ENGLAND, UNITED KINGDOM
...the successful development of the Alvita range and delivery of the NPD Plans on budget. Key Responsibilities: You will manage the regulatory tasks in launching multiple NPD projects by the budget and 5-year growth plan. You will support the Alvita European Brand Manager and Central...
Continuous Improvement PMO
, , 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...
QPPV office and Alliance Management
GREATER LONDON, ENGLAND, UNITED KINGDOM
Passionate about transforming lives? Ready to drive innovation in Research & Development? We're on a mission to revolutionise patient care and need your expertise to make it happen. QPPV Office & Alliance Manager (f/m/d) What You'll Do: Lead global Pharmacovigilance system with finesse...
Senior Manager, Quality
ABINGTON PIGOTTS, ENGLAND, UNITED KINGDOM
...oversight for Bicycle s development programs, ensuring compliance with applicable ICH GCP and GLP standards and global regulations. As an integral member of the team tasked with product development, the position serves as a Quality and compliance business partner, engaging with multiple...
Clinical Trial Manager - Global Pharma - Complex Trials
UNITED KINGDOM, , UNITED KINGDOM
...within Virology development. You will be apart of significant growth within its pipeline in Virology through internal research, partnerships and acquisitions. The Role: Provides regional management of global PIb-III studies managed by Clinical Program Manager Drafts and coordinates review...
! Regulatory Affairs Manager - Remote/hybrid in Uxbridge - Global Biotech !
UXBRIDGE, ENGLAND, UNITED KINGDOM
...Team (GRT) Global Development Team (GDT) Clinical Study Team (CST) Label Working Group (LWG) Regional Teams (e.g. IMT, IBT, NAMT) Act as a contact with relevant regulatory agencies in fulfilling local obligations by product assignment Document and communicate details and outcomes of...
MSL - small Pharma
, , UNITED KINGDOM
...Engaging with guideline development and revision through scientific exchange and support. Developing and managing KOLs including KOL identification, engagement and support. Please apply in order to receive the full job description. Remuneration: The successful candidate would receive a...
! RBDS Supervisor based in Andover - Leading Chemical manufacturing!
, , UNITED KINGDOM
...training and development plans ensuring that we are correctly resourced and trained to meet our customers needs. Although highly regulated and technical, this is a fast paced environment requiring a high degree of flexibility and problem solving. Building close working relationships...
Automation Project Manager - Global Pharma - Perm
WATFORD, 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...
Production Technician
MILTON KEYNES, 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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