Are you a business? Hire pharmacovigilance candidates in London
CK Group are recruiting for a Medical Territory Account Manager to join a world leading manufacturer of dialysis equipment, to cover a UK territory (London and South of the UK) on a permanent basis. This role would involve travelling 3-4 days/ week with overnight stays. The Role: Under the gui...
The Quality Specialist position supports the delivery of Medical Information and Pharmacovigilance services, to assure ongoing compliance with quality and industry regulatory requirements. The Quality Specialist performs improvement activities through continuous monitoring and evaluation of the q...
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 ...
Role: Global Labelling Lead Location: United Kingdom - Remote Salary: Very competitive salary on offer Planet Pharma are supporting a leading global biotech company with the search for a new Global Labelling Lead to join them during an exciting period of growth! Perfect for someone looking to uti...
Title: Clinical Trial Manager - Global Pharma - Complex Trials Location: London Duration: Full Time Salary: Competitive Based on Experience We’re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. Y...
BioTalent is headhunting for a UK or Germany based Senior (Global) Drug Safety Physician who is fluent or business level professional in both English and French language. The role is remote with the option of office sites (in UK and Germany) to work from. Responsibilities: Lead clinical safety ac...
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest ...
Define, develop, and leads regional strategies to maximise regulatory and pharmacovigilance success. Effectively communicate the likelihood of pros and cons to Management. * Sound knowledge on ...
As a Pharmacovigilance Specialist, you will be responsible for performing pharmacovigilance-related activities for all of the company's products and ensuring the company is compliant with all the ...
UK owned they are now expanding and are looking to recruit a Pharmacovigilance Co-ordinator. Job Description: * Develop and approve artwork components and patient information (SPC, PIL, cartons and ...
Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural ...
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 ...
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 ...
Enter and maintain data in the Pharmacovigilance Database. * Monitor adverse events received via EEDR. * Generate safety data for signal detection and periodic aggregate reports. * Supply safety data ...
Lead global Pharmacovigilance system with finesse, ensuring compliance and efficiency. * Dive deep into international agreements, safeguarding Pharmacovigilance standards. * Craft and negotiate Drug ...
BSc, MSc or PhD in Biochemistry/Chemistry/Pharmacology/Pharmacokinetics and likely be highly experienced (>10 years) in the pharmaceutical industry * Expert knowledge are DMPK concepts such as Tier 1 ...
... and pharmacovigilance success. * knowledge of requirements of MA Transfer in EU territories, which includes requirements of notarization and translations. * a team of 4 to ensure day-to-day ...
Phil in biology, pharmacology, toxicology or a related discipline · Peer-reviewed research publications commensurate with career stage · Background in working on monogenetic disease modelling, in ...
Liaise with the External Pharmacovigilance consultants for submission of Safety variations and PSUSA Variations. * Working with specialist computer software and resources; (Eg: ectd). * Experience in ...
Actively participating in and supporting required QMS activities, including complaint and pharmacovigilance reporting. Your Background * Degree qualified in life science or equivalent. * Experience ...
Pharmacologist // Gene-ious new cancer target // London You have industrial, hands-on lab experience within cancer drug discovery. How would your work have its greatest impact? Would it be designing ...
You will support the European Head of Regulatory Affairs and Pharmacovigilance in specific projects related to Alvita, including assessing the launch in new territories or the development of new ...
Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...
Experience and expertise working on Lead Optimisation programs, with familiarity of optimisation of Drug Metabolism and Pharmacokinetics (DMPK). * Experience of working with and closely managing CRO ...