The function of this role is to be responsible for the performance of bioanalytical studies in support of human or animal health drug development.
You will act as the single point of study control and will have overall responsibility for the scientific, technical and regulatory conduct of studies allocated as well as for the interpretation, documentation and reporting of results. Close and regular liaison with the client is of primary importance. Dependant on experience, the scientist may manage complex customer programmes with multiple studies and/or have managerial responsibilities for other scientists.
You will ensure the study is performed in accordance with regulations and study protocol, achieve delivery targets by assessing deadlines, timescales, anticipated problems and costings as well documenting and handling all study communication and advising clients on study designs.
Suitable candidates will have proven industry experience working within the field of protein analytical chemistry (management of analytical teams or project management) in a regulatory environment (GLP/GCP/GMP). In addition, experience of client management and technical expertise in a relevant scientific arena is required. Experience in LC/MS/MS and method development would be a distinct advantage.
To apply for this position, candidates must be eligible to live and work in the UK
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