Gerrards Cross45-55K plus excellent pension, benefits, bonus

New opportunity with a rapidly expanding Global pharmaceutical company.

You will develop study implementation plan and manage operational aspects of clinical trials, including assignment of specific tasks to in-house CRA’s.

You will interact with CRO’s, other external vendors and various non-clinical functions within the organisation, in order to meet company timelines and obtain Regulatory approval of NDA submissions.

This is an exciting opportunity that is a new role to the business, allowing you the opportunity to develop and take your career to the next level.

Demonstrable experience in Clinical Development in Europe gained with in a pharmaceutical, biotech or CRO company is essential. In addition to this you will have a complete knowledge of GCP, FDA and ICH Guidelines. Therapeutic experience in diabetes or CVS is desirable, but other therapy areas will be considered.

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