Study start up Specialist/Study Start up Associate, Belgium
The opportunity for a Global Study Start up Specialist is a key role within my clients clinical research and regulatory teams, which combines the coordination of clinical documentation with the regulatory process involved in filing and submissions to local and global ethics committees. As such, my client are looking for an individual who can be based out of their Brussels office that would be looking for a more varied position.
This opportunity is ideal for a Senior CRA/Senior Clinical Research Associate/SCRA looking to dramatically reduce their travelling whilst enhancing the experience they have already honed, or a country Study Start Up Specialist/Country Study Start Up Specialist that would like to broaden their geographic remit.
Day to day responsibilities of a Global Study Start Up Specialist include, but are not limited to;
- Acting as primary contact with investigative sites during site start-up activities (i.e., site identification, selection and activation)
- Support Business Development, Project Manager/Clinical Manager by assessing project feasibility,
- Work closely with investigative sites to negotiate and finalise investigator contracts and budgets
- Oversee the clinical trials set-up
This opportunity is office based and offers a highly competitive basic salary and benefits package, whilst working with one of the industries most stable employers.
For more information call Bernardo Reveco on +44(0)207 940 2105 or email your latest CV to firstname.lastname@example.org for more information.
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