Global Contract Testing company
Highly competitive salary plus bonus
Based in Manchester
A Global Contract testing company are looking to add an additional Study Director to their team in Manchester. The successful candidate will work alongside 3 other Study Directors with this role existing due to growth.
The client offers a defined career progression plan with lots of opportunities to represent the company at conferences and meetings as well as travel to customer sites.
The ideal candidate will have experience in GLP as well as cGMP. You will be responsible for drafting client study plans and managing a number of client studies at any one time.
Good organisation and communication skills are key in this role as is the ability to "spin lots of plates".
A good Chemistry Technical background is key to being a success in this role across the standard Chromatography disciplines e.g., GC, LC etc.
Any additional experience in Mass Spec - Triple Quad (QQQ), Time Of Flight (TOF) would be highly desirable however the Analytical teams themselves are experts and can help provide input into any technical terms for client reports where and when required. The ability to Project Manage together with a Chemistry background is more essential.
This role could suit someone who is an experienced Senior Analyst with experience of managing multiple projects looking to progress their career or an experienced Study Director who is looking to change roles and work for one of the world leaders in their field.
Your day will consist of writing and designing study plans, reporting data back to clients, collaborating with the other departments, maintaining contact and updating clients on progress, working with the commercial team as well as the Subject Matter Experts to provide a full service to the company's clients.
Being up to date with current regulations is also a key part of this role - ISO 17025, GLP and cGMP as well as to the usual H&S regulations and standards.
Qualifications and Experience:
A minimum of a Degree in a Chemistry related field to give a basis to build from together with additional experience working to GLP and / or cGMP.
If this sounds like you or you would like more information please do not hesitate to get in touch.