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Work for a leading biotech company which is poised to launch key products in Europe, this established team is expanding and keen to find able study managers who are experienced in supporting Phase I-III projects globally for two key programmes.

The open permanent role will suit competent self starters who are satisfied to work at this level and function as a support for the Program Leads but not take the helm personally. Maturity, breadth of experience and skilled team playing ability are key to success through this busy period of change; there is good scope for developing knowledge across Phases as well as new molecules come into the clinic. You will have proven skills in managing project delivery of studies outsourced to CROs andenjoy the co-ordination and oversight such work involves. EXpertise in designing and managing Phase I/PoC studies is desirable for one role.

This is an exceptional chance to work in a more dynamic well funded company environment where you can contribute beyond project and grow in stature. You will be free to create innovative project approaches within a global framework and learn about working with all types of stakeholders as the company progresses through registration and launch.

Qualifications:

Life science, nursing or higher degree.
Competence in Study Management in Phases I-III
Ability to travel to work with partners, peers and sites to enable success in compliance and delivery
Flexibility to travel periodically

Terms and^conditions are exceptional and planned company growth will allow progression in time as the company moves new NCEs into Phase I. The role is office based on the M40/A34 axis.

Relocation support is available for homeowners and those moving to the^splendid location.