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- Assisting with the monitoring & evaluation of safety profiles for allocated products to ensure that optimal decisions are made at all stages of the product lifecycle.
- 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 documentation is accurate & available to meet global compliance & regulatory requirements.
- Bachelors degree in Biomedical or Health Care related speciality or equivalent experience.
- Experience in scientific literature review, data gathering, data synthesis, analysis and interpretation.
- Competent medical/scientific writing skills.
- Sound computing skills Knowledge of relevant pharmacovigilance regulations & methodologies.
- Knowledge and experience of the principles of causality assessment and the evaluation of safety signals.
- Basic understanding of the HIV therapy area would be an advantage.
Clinical Safety Scientist - Brentford, United Kingdom - CK Group
Description
CK Group are recruiting for a Clinical Safety Scientist to join a company in the pharmaceutical industry at their site based in Brentford on a contract basis for 12 months.Salary:
Up to £40.00 per hour PAYE. This role is inside IR35.
Clinical Safety Scientist Role:
Our client is a one of the largest global healthcare companies researching, developing and supplying innovative medicines, vaccines and healthcare products with their global headquarters in the UK. They invest around £1bn in research and development in the UK annually.
Location:
This role is based at our clients site in Brentford.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference T56817 in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.