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Outsourcing Oversight Manager
49579
ENGLAND, BERKSHIRE, BERKSHIRE, UK, BERKSHIRE, BERKSHIRE
...Familiarity with Pharmacovigilance and drug development. Basic knowledge or experience with aspects of outsourcing and/or vendor oversight. Ability to interpret, analyze, and present scientific and medical data. Comfortable with medical terminology and American Medical Association manual of...
Global Quality Manager
WINDSOR, GB
Excellent opportunity to join a leading pharma company as a Manager - Global Quality Management. The main task is to manage and perform audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the inspection management, the...
Director, Neuroscience Pharmacology (Remote)
OXFORD, ENGLAND, GB
...to regulatory, pharmacovigilance and medical affairs documents as required to meet corporate needs Contribute to Function and/or Project Teams as determined within the governance matrix structure Has overall control of planning, budgeting, managing expense priorities, and recommending and...
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Global Quality Manager
WINDSOR
...audits with focus on Pharmacovigilance audits. Additional tasks are to support the continuous improvement of Quality System, the inspection management, the regulatory intelligence activities, the SOP and WP management, the validation activities and the project liaison activities. /p p Key...
Financial SSU PM (home-based)
50958
MAIDENHEAD, BERKSHIRE, MAIDENHEAD, BERKSHIRE
...Regulatory Affairs, PharmacoVigilance, Business Compliance, Legal and regional operations, Head Quarter functional areas and externally with vendors and sites, budgets, CTRAs and local milestones. Collaborates closely with Regional Operations to align country timelines for assigned...
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Chief Medical Officer/Chief R&D Officer - Africa Clinical Research Network
OXFORDSHIRE, GB
...data management, pharmacovigilance and beyond Craft a bold research agenda that addresses Africa's most pressing health needs, with a focus on delivering affordable, accessible and scalable innovations Build and oversee a portfolio of sponsored and investigator-initiated trials across the...
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...
Supply Chain Associate
SURREY, GB
...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...
Supply Chain manager - Serialisation
SURREY, GB
...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 Education Manager - Medical Device
CROYDON
...including complaint and pharmacovigilance reporting. /li /ul ol li Job Requirements: /li /ol p br /p p strong Education and Experience: /strong /p ul li Registered Nurse qualification. /li li Minimum 24 months of experience in Intensive Therapy Unit (ITU). /li li Proficiency in...
Supply Chain Associate
SURREY
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /u /p p br /p p u We are an equal opportunities Recruitment Business and Agency. /u /p p We welcome applications from all suitably qualified...
Supply Chain manager - Serialisation
SURREY
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p u We are an equal opportunities Recruitment Business and Agency. /u /p p We welcome applications from all suitably qualified candidates...
Head of Global Safety Data Integration and Literature (UK)
£80 - 100
SLOUGH
...team in the Product Pharmacovigilance & Device Safety team, ideally based in our Raleigh (US), Monheim (Germany), Slough (UK) or Brussels (Belgium) offices. /p p b About the role: /b /p p You will play a pivotal role in oversight and implementation of new and improved solutions to...
Clinical Education Manager - Medical Device
CROYDON, UNITED KINGDOM
...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...
Senior Regulatory Affairs Officer
31996
KENT
...EMC MHRA CESP Pharmacovigilance Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications for any applicant who fulfils the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is...
We've expanded the search to "England" to find more jobs with all your keywords
Senior Director, Pharmacovigilance Intelligence
44527
UXBRIDGE, LONDON , UXBRIDGE, LONDON
We are looking to add a new critical reporting directly to the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating...
Senior PV Operations Scientist - Permanent Position
36929
HATFIELD, HERTFORDSHIRE, HATFIELD, HERTFORDSHIRE, AL10 9SN
...experience in a Pharmacovigilance role. Prior experience with SDEAs and building relationships with PV partners. In depth knowledge of Pharmacovigilance regulatory reporting requirements in European countries Graduate level education preferred (life sciences, pharmacy or nursing degree...
Senior Director, Global Patient Safety - Gene Therapy
62571
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...as gene therapy into pharmacovigilance practices Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required. Function as a subject...
Clinical Scientist
47594
LONDON , LONDON , LONDON , LONDON
...trends. Manage pharmacovigilance processes for SAEs and adverse events of special interest (AESI). Work with data management and clinical operations to ensure data entry meets requirements. Oversee any regulatory reporting or actions required. Update Drug Safety Update Report (DSUR) and...
Senior Director, Global Patient Safety - Ophthalmology
61932
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required. Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest. Familiarity...
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