Clinical Trial Applications Manager - £40k

This is a varied role within a newly established international site services function!

Working on an international level you will be responsible for the co-ordination and preparation of clinical trial applications for submission to international ethics committees. You will work closely with the group director to establish processes and systems for this centralised applications service and will have the opportunity to recruit and manage application specialists who will co-ordinate the day to day preparation of essential documents. As the international contact for CTA and LREC/MREC applications you will work closely with operations, project management and regulatory colleagues on a daily basis to co-ordinate the submission and retrieval of essential documents. Process improvement and training will also be part of your remit. Excellent benefits are available along with the opportunity to contribute to the growth of a new and centralised applications function!

This position would suit an experienced lead CRA or project manager with extensive experience of trial and ethics applications on an international level. At least five years CRO experience is required along with two years in a supervisory role. A working knowledge of project management techniques and timeline management using MS Project is essential. You must be able to travel periodically and a strong communicator who is comfortable working in a high pressure and changing environment.

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