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The Clinical element of drug development encompasses all aspects of the clinical trials process; from first in human studies through submission and drug/device approval (phases 1-4). Experts working in this space usually specialize in certain therapeutic areas, as the study design in some spaces differs to others. There are many individuals involved in the various drug/device development phases, to include Biostatisticians, Medical Directors and Data Managers.
Our specialism breakdown includes:
Clinical Trial Managers
Regulatory Medical Writing
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Clinical Compliance Director
- £140000 - £150000 per annum
SciPro are currently recruiting a new Clinical Compliance Director to support the extensive number of clinical studies currently being undertaken by this international biotech who is looking to support patients with unmet orphan diseases. If you are an experienced QA professional will have an extensive knowledge of ...
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