Clinical Safety Scientist
Posted 19 hours 7 minutes ago by CK Group
Permanent
Not Specified
Other
Not Specified, United Kingdom
Job Description
CK Group are recruiting for an Clinical Safety Scientist, to join a company in the pharmaceutical industry, on a contract basis for 6 months. This is a fully remote position.
Salary:
£555 per day Umbrella or £430.17 per day PAYE.
Clinical Safety Scientist Role:
To provide safety support and expertise with particular focus on medicines for the treatment and prevention of HIV. The key focus is on safety, evaluation and risk-management.
This position is responsible for signal detection, and evaluation activities for assigned products.
Further Responsibilities Include:
Your Background:
Company:
Our client is 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:
Fully remote.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Salary:
£555 per day Umbrella or £430.17 per day PAYE.
Clinical Safety Scientist Role:
To provide safety support and expertise with particular focus on medicines for the treatment and prevention of HIV. The key focus is on safety, evaluation and risk-management.
This position is responsible for signal detection, and evaluation activities for assigned products.
Further Responsibilities Include:
- Authoring the SERM safety contribution to global regulatory submissions in partnership with the product physician.
- May respond to auditors/inspectors requests for information/additional information and completes corrective and preventative actions (CAPAs) within agreed timelines.
- Driving production of regulatory periodic reports and associated documentation and RMPs globally.
- Assist in authoring periodic regulatory documents (PSURs PBRERs , DSURs, licence renewal documentation) according to the agreed process and timelines.
- Assists in the update of investigator brochures.
Your Background:
- Bachelors, or above, degree in Biomedical or Health Care related speciality.
- 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 and methodologies applicable to SERM activities.
- Knowledge and experience of the principles of causality assessment and the evaluation of safety signals.
Company:
Our client is 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:
Fully remote.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.