Pharmacologist jobs in Wembley

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 ...

Pharmacology Expert Reports to: Head of Chemical Biology STP This is a full-time, permanent position on Crick terms and conditions of employment Overview The position is within the Chemical Biology ...

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 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 ...

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 ...

The individual will also partner with internal teams such as pharmacovigilance, local in-country teams, and the device quality assurance team to ensure the appropriate and accurate reporting of ...

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 ...

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 ...

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 ...

Lead global Pharmacovigilance system with finesse, ensuring compliance and efficiency. * Dive deep into international agreements, safeguarding Pharmacovigilance standards. * Craft and negotiate Drug ...

... 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 ...

Actively participate and support required QMS activities, including complaint and pharmacovigilance reporting. To succeed in this role, you will need to come from a registered Nurse background, with ...

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 ...

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

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

The healthcare division works across multiple topic areas within both pharmacology and healthcare. This role sits within their general medicine team which covers a range of healthcare projects but ...

The healthcare division works across multiple topic areas within both pharmacology and healthcare. There are two teams which allow you to either focus on a therapy area you are passionate about or ...

Holds a degree in medicine, pharmacy, biology, chemistry, pharmacology, or a related life sciences discipline.

PhD or MSc (with equivalent experience) in a relevant field (e.g., Biology, Biochemistry, Pharmacology, Physics, Engineering) * 6+ years of industry or postdoctoral experience. * Experience in ...

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

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

... and Pharmacovigilance · Supports more complex complaints that are escalated. · Serve as a Subject Matter Expert for a designated product(s) within the team when required. · Where applicable ...