Search Results: 6 vacancies
£42k - £57k per annumEstimated
...knowledge and close relationships with our clients and the wider industry really make us unique in our field. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We welcome...
Suggested
Permanent employment
Full time
For contractors
Work at office
Immediate start
Remote job
£35k - £47k per annumEstimated
...knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We welcome...
Suggested
Permanent employment
Full time
For contractors
Work at office
Flexible hours
£35.39k - £42.62k per annum
...implementing appropriate audit and monitoring systems and performing risk assessments for each study.
Implementation of appropriate pharmacovigilance / adverse event reporting systems in compliance with EU and national regulations.
Maintaining trial documentation in...
Suggested
Permanent employment
Work at office
Local area
Flexible hours
£35.39k - £42.62k per annum
...implementing appropriate audit and monitoring systems and performing risk assessments for each study. Implementation of appropriate pharmacovigilance / adverse event reporting systems in compliance with EU and national regulations. Maintaining trial documentation in accordance...
Suggested
Permanent employment
Full time
Local area
£94k - £127k per annumEstimated
...bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal...
Suggested
Permanent employment
Full time
For contractors
Work at office
Immediate start
Remote job
£36k - £49k per annumEstimated
...for our commitment to excellence and service delivery.
We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities...
Suggested
Permanent employment
Full time
For contractors
Work at office
Flexible hours
