Pharmacovigilance jobs in Croydon

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 ...

About the role The Associate Director, Clinical Pharmacology is responsible for leading clinical research activities with focus on clinical pharmacology phase I pharmacokinetics and bioequivalence ...

Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural ...

Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners ...

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 ...

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 ...

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 ...

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 ...

Actively participating in and supporting required QMS activities, including complaint and pharmacovigilance reporting. Your Background * Degree qualified in life science or equivalent. * Experience ...

You will collaborate and interact with scientists across groups within our company, who have extensive experience in neurodegeneration, cellular biology, in vitro pharmacology, chemistry, and data ...

Collaborating with members from other functional areas, including medicinal chemistry, in vivo and in vitro pharmacology, imaging, genetics, and translational sciences to drive progress * Timely ...

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 ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Key Words: Absorption, Distribution, Metabolism, Excretion, ADME, Drug Metabolism, Pharmacokinetics, DMPK, Small Molecule, Drug Discovery, Pharmaceuticals, In Vitro, Cell-based Assay, Metabolic ...