save this search
Adverts by Google
We've expanded the search to "Hillingdon" 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...
Car Fleet Manager
HAYES, 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...
Car Fleet Manager
HAYES
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /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...
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
HAYES, 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...
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...
Adverts by Google
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...
Director, Global Patient Safety Sciences - Hematology
80469
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. A proven...
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...
We've expanded the search to "London" to find more jobs with all your keywords
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...
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...
PV Consultant
LONDON, GB
...for: Day-to-day pharmacovigilance oversight : Review SAEs and queries to investigators on a regular basis, support the data cleaning for safety data, and oversee signal management to identify significant trends. Case processing : Manage PVG processes for serious adverse events (SAEs) and...
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...
Patient Safety Specialist
LONDON, GB
...experience with documentation would be advantageous. Skills & Knowledge: Knowledge of national and international regulations for pharmacovigilance Knowledge of pharmacological and medical terminology Good communication and interpersonal skills Quality and results oriented. Computer...
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...
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...
Senior Director, Medical Affairs & Clinical Development
68922
LONDON,
...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...
PV Consultant
LONDON
...li strong Day-to-day pharmacovigilance oversight /strong : Review SAEs and queries to investigators on a regular basis, support the data cleaning for safety data, and oversee signal management to identify significant trends. /li li strong Case processing /strong : Manage PVG processes for...
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...
Medical Information Specialist (German Speaking) - Science Graduates - Home based in UK!
WFH
...Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. /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...
Medical Director – Medical Affairs & Clinical Dev
£200 +
LONDON
...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. /p br br...
Adverts by Google