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Pharmacovigilance development jobs

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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...
Clinical Nurse Advisor 41266 SLOUGH, BERKSHIRE, SL1 ...plans, activities and developments and to exchange knowledge and experience within the team. Client Focus To communicate with and develop relationships with key health care professionals at all specified sites, whether hospital, home or other establishments who have opted in for the service...
Looking for Pharmacovigilance Development 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.
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...
Manager, Global Aggregate Reports quality and compliance BERKSHIRE, ENGLAND, UNITED KINGDOM The Manager, Global Aggregate Reports Quality and Compliance is an integral member of the Global Aggregate Report office and PV Writing Organization. The position holder responsibility includes the entire CSL product portfolio and development pipeline. Responsibilities include: - Acts as a...
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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...
Pharmacovigilance Manager WINDSOR, ENGLAND, UNITED KINGDOM Job Title: Quality Manager, Global Quality Management Location: UK (preferably located near Windsor) Are you a Pharmacovigilance professional with a keen eye for quality management? Do you possess experience in audits, inspections, and CAPA management, and aspire to transition into a broader...
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...
Director, Pharmacovigilance Case Processing 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. Director, Pharmacovigilance (PV) Case Processing...
Senior Safety Physician UNITED KINGDOM, , UNITED KINGDOM ...or still in clinical development. Your role will involve leveraging your medical expertise and extensive knowledge of pharmacovigilance (PV) legislation to contribute to our team. We are looking for an individual who excels in analytical thinking, can navigate complex data, establish structured...
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...
Director, Drug Safety Lead , , 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...
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...
Technical Support Analyst UNITED KINGDOM, , UNITED KINGDOM Company: Generis Enterprise Technology Limited Job Title: Technical Support Analyst / Support and Development Liaison (Remote) Location: Remote UK Contract Status: Full-time / Permanent Staff About us Generis is a fast growing and successful UK-headquartered developer of world-class Content and...
Automation Engineer HERTFORDSHIRE, 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...
Clinical Data Programmer 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...
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...
IT Manufacturing Project Manager , , 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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