Health and Manager
6 days ago
Permanent Location: Friday 25 Oct 2024 17:00 The Clinical Study Director will work in a quality focus environment regulated to GLP standards.
The successful candidate will lead, manage data and report non-clinical and clinical studies for safety and efficacy trials for animal health products.
The successful candidate will be responsible for the planning, conduct and reporting of studies in an organised and timely manner, and in accordance with Regulatory requirements (e.g.
The Clinical Study Director will be the single point of control for a range of study deigns, including Pharmacokinetic/Bioequivalence studies, residue determination, Target Animal Safety, Clinical studies (artificial and natural infections).
The Study Director is responsible for ensuring the scientific, administrative and regulatory aspects of the study are controlled.
Overseeing data collection and analysis is conducted and reported in line with the approved SOPs, Method and Protocol.
Receive and evaluate data and phase reports for inclusion in the Final Study Report.
Ensuring that the study is conducted in compliance with the relevant regulatory standard and Drawing the final overall conclusions of the study.
Experience in scientific report writing and review.
Experience in managing multiple projects.
Flexible with a proven ability to adapt as projects progress through development.
Excellent time management skills.
Proven ability to prioritise and deliver to project deadlines.
Have a full UK driving licence.
Previous experience in a laboratory with knowledge of bioanalytical method testing.
An understanding of relevant regulatory guidelines.
Norbrook Laboratories Limited employs a workforce with members of all sections of the community and is committed to appointing people purely on the basis of merit.
In accordance with our equal opportunities policy, we would particularly like to welcome applicants from the Protestant Community.
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