Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural ...
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 ...
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 ...
Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners ...
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 ...
Employers want to know
Do you have work experience?
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 ...
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 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 ...
Acts as a Triage Manager, performs impact assessments of evolving pharmacovigilance legislation and regulatory guidance in safety sciences, e.g., aggregate reporting, literature review, signal ...
Lead global Pharmacovigilance system with finesse, ensuring compliance and efficiency. * Dive deep into international agreements, safeguarding Pharmacovigilance standards. * Craft and negotiate Drug ...
The role requires expertise in in vitro assay development, molecular pharmacology, and cell biology. As a Principal Scientist, you must also have a strong leadership background. Key Responsibilities
... 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 ...
Actively participating in and supporting required QMS activities, including complaint and pharmacovigilance reporting. Your Background * Degree qualified in life science or equivalent. * Experience ...
... 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 ...
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 ...
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 ...
Following and creating operational procedures as it relates to pharmacovigilance workflows, order processing, logistics, regulatory scoping, client set-up documents, etc * Be responsible for program ...
Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...