save this search
Adverts by Google
We've expanded the search to "Hillingdon" to find more jobs with all your keywords
Car Fleet Manager
HAYES, 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...
Senior Director, Pharmacovigilance Intelligence
UXBRIDGE, GREATER LONDON, HILLINGDON, GREATER LONDON; LONDON; ENGLAND, UK
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...
Car Fleet Manager
HAYES
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p We are an equal opportunities Recruitment Business and Agency. /p p We welcome applications from all suitably qualified candidates regardless...
Looking for Pharmacovigilance jobs in West Drayton?
Top Salaries! Full time, part time and contract.
WEST DRAYTON
Visit PerfectJobs4U UK for the widest selection of top UK jobs. Full time, part time and work from home roles.
Car Fleet Manager
LONDON (HAYES), SOUTH EAST ENGLAND
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /p p br /p p We are an equal opportunities Recruitment Business and Agency. /p p We welcome applications from all suitably qualified candidates...
We've expanded the search to "West London" to find more jobs with all your keywords
Qualified Person for Pharmacovigilance (QPPV - UK)
HARROW, GB
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...
Adverts by Google
Director, Senior Director & Executive Director, Safety Physician SERM (Safety Evaluation & Risk Management)
68762
BRENTFORD
...PV Expertise Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix. Leads the safety component of global regulatory submissions. Expert evaluation skills and analytical thinking for literature review, clinical...
We've expanded the search to "London" to find more jobs with all your keywords
Manager, Pharmacovigilance and Medical Information - FTC
LONDON, GB
JOB DESCRIPTION Job title: Manager, Pharmacovigilance and Medical Information - FTC Reporting to: Director, Scientific Affairs Department: Scientific Affairs CNX Therapeutics is a European pharmaceutical company dedicated to improving the lives of patients through the supply of essential medicines...
Key Account & Access Manager - Diabetes
LONDON, GB
...reporting in this area. Pharmacovigilance-Reporting: The Biocon employee should follow and apply within 24h the standard Biocon PV approach if becoming aware about adverse events/side effects and/or incidents including lack of efficacy for Biocon products. Pharmacovigilance department by any of...
Urology - Key Account Manager
LONDON, 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...
Senior Director, Medical Affairs & Clinical Development
LONDON, GB
...regulatory affairs, and pharmacovigilance processes. Demonstrated track record of successful product launches and lifecycle management strategies. Excellent communication and presentation skills, with the ability to effectively engage with internal and external stakeholders. Proven leadership...
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...
Clinical Education Specialist
£50000 - £55000 per annum , GBP
LONDON
...including complaint and pharmacovigilance reporting. To succeed in this role, you will need to come from a registered Nurse background, with ITU experience. You will need a working knowledge of CRRT. Experience in teaching/supporting in a class-room based and clinical environment. Apply: It is...
Director - Vault Safety Suite
LONDON, ENGLAND, UK
...understanding of the Pharmacovigilance function, related business processes, and the associated software applications used to collect, process, analyze and report data and manage related documents. This role is responsible for contributing to our Software Product Strategy while growing Veeva s...
Medical Director, UK & Western Europe
LONDON, ENGLAND, UK
...Only Medics/Clinical Professionals) is a specialist division that focuses exclusively on recruitment of Medical Affairs, Clinical Development & Pharmacovigilance for pharmaceutical companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory Authorities...
Medical Director - Medical Affairs & Clinical Dev
LONDON, ENGLAND, UK
...Only Medics/Clinical Professionals) is a specialist division that focuses exclusively on recruitment of Medical Affairs, Clinical Development & Pharmacovigilance for pharmaceutical companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory Authorities...
Associate Medical Director, Immunology
LONDON, ENGLAND, UK
...Only Medics/Clinical Professionals) is a specialist division that focuses exclusively on recruitment of Medical Affairs, Clinical Development & Pharmacovigilance for pharmaceutical companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory Authorities...
MSL Lead - Cross Portfolio Leadership
LONDON, ENGLAND, UK
...Only Medics/Clinical Professionals) is a specialist division that focuses exclusively on recruitment of Medical Affairs, Clinical Development & Pharmacovigilance for pharmaceutical companies, biotechnology companies, Clinical Research Organisations (CROs) and Regulatory Authorities...
Account Manager (Permanent)
LONDON, ENGLAND, UK
...including complaint and pharmacovigilance reporting. Your Background Degree qualified in life science or equivalent. Experience of working in a relevant hospital sales role and full UK driving license. ABPI qualified understands the ABPI code of conduct and applies it accordingly. A nursing...
Clinical Education Specialist (Permanent)
50000 - 55000
LONDON, ENGLAND, UK
...including complaint and pharmacovigilance reporting. To succeed in this role, you will need to come from a registered Nurse background, with ITU experience. You will need a working knowledge of CRRT. Experience in teaching/supporting in a class-room based and clinical environment. Apply: It is...
Automation Engineer
LONDON, ENGLAND, UK
...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...
Adverts by Google