GLP Bioanalytical Study Director

North Yorkshire
Dependent on experience
15 Oct 2019
12 Nov 2019
Debra Fong
Contract Type
Full Time
Are you an experienced GLP Study Director looking for a new exciting opportunity?

We are currently looking for a GLP Study Director to join a leading contract testing company based in the North Yorkshire area.

As the GLP Study Director you will be expected to help the company directors implement and manage the principles of GLP, GCP and health and safety compliance within the company and advise other bioanalysts and the Laboratory Head in maintaining an efficient, safe, GLP and GCP compliant laboratory.


Your duties as the GLP Study Director will be varied however the key duties and responsibilities are as follows:

1. As the Study Director, you will be all of the study data (validation, analytical and equipment studies) as well as supervise staff performing the laboratory work, draft study and validation protocols, review all study data for accuracy and GLP / GCP compliance as well as transfer study data into reports.

2. As well as study directing, you will be involved in personnel training and development for performing quantitative analysis using LC-MS and multiplexed immunoassay whilst providing assistance in the technical, scientific, practical and GLP and GCP compliance of all work in the company.

3. Additionally, alongside the study directing responsibilities, you will have to prepare proposals for major capital investment for authorisation by the Directors, represent the company at internal and external meetings as well as perform QC procedures for studies performed by other Study Directors or analysts.

4. Lastly, you may be required to help with recruitment, staff selection, performance assessment, training and development as well as setting and assessing staff performance standards and objectives.


To be successful in your application to this exciting opportunity as the GLP Study Director we are looking to identify the following on your profile and past history:

1. Relevant Life Sciences degree and experience using LC-MS for analysis in a GLP regulated CRO laboratory is essential.

2. Proven industry experience in study directing, managing projects or writing reports would be beneficial, however, not essential, as this role is also open to those looking to step into a Study Directing position.

3. You will need to have had hands on experience working in a regulated environment, following SOPs, protocols and ensuring Health and Safety regulations within a laboratory.

Key Words: GLP Study Director | Study Manager | LC-MS | Chemistry | Contract Testing Laboratory | Analyst | Clinical Testing

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.

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