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Mass Spectrometry, Analytical, Chemical, Laboratory,

Covering the following locations: Cambridge, Leicester, Milton Keynes, Northampton, Peterborough, Stevenage

Assistant Project Manager - Chemistry Department
This position is full time and one year fixed term.

The Rushden site is a centre of excellence for Radiolabelled Sciences incorporating Metabolism, Bioanalysis and Chemistry. The Chemistry team is responsible for the synthesis and analysis of isotopically labelled compounds for our Clients for use in non-clinical and clinical drug development studies often under GMP conditions. The Project Management team within Chemistry manages the projects and act as the main point of contact for clients to aid the smooth delivery of isotopically labelled compounds.

A passionate business with a strong appetite for growth and innovation, we are proud of our achievements to date and excited for what the future brings. To continue our growth and success, we are looking for a temporary Assistant Project Manager to shadow and assist the Project Manager in the running of individual radiochemistry projects liaising both externally with clients, and internally with other departmental functions. The Assistant Project Manager will be expected to develop to a level where projects can be managed with minimal assistance from the Project Manager/Senior Project Manager.

Key roles and responsibilities
- To assist in the overall project management of individual projects, liaising both externally
with Clients/ Clinics and internally with QA/ QC/ Production/ Metabolism where required.
- To provide cover for the Senior Project Manager/ Project Manager when required.
- Attend and minute co-ordination meetings between QA and QC departments and
production and QC departments.
- To prepare individual radiochemistry Gantt charts on a project by project basis for Clients.
- Supply Cardiff radiochemistry with information on labelled intermediate requirements for
clinical chemistry projects.
- Collect and distribute methods/ materials for method verification/ trial synthesis work.
- Involvement in teleconferences and e-mails to clarify and finalise project work or discuss
any issues arising.
- Provide radio synthesis information for incorporation into the IMPD/IND section of the CTA.
- Production of stability protocols and final results tables and reports for client review.
- Generate product specification sheets based on proposal information for internal and Client
- Participate in dose selection meetings if needed.

Education, skills and experience
- Must hold a scientific qualification along with a sound understanding of both synthetic and
analytical chemistry
- Full training for the role will be given but an interest/basic understanding of GMP (Good
Manufacturing Practice) would be useful, but is not essential
- Proficient with Microsoft Office packages (Outlook, Excel, Word)
- Excellent verbal and written communication skills
- Must be confident and have a friendly approach

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* Salary Guide
Job Ref: 65282

Liam Whelan

Executive Recruiter +44 1494 818 027

James Higgins

Scientific Resourcer +44 1494 818 009

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