Support in drafting, negotiating, reviewing and processing contracts and economic reports of collaborations and research projects.
Support in writing, reviewing the economic memories of academic studies.
Obtaining approvals and tracking regulatory documentation for academic studies.
Notifications to Ethics Committees and AEMPS throughout the study.
Preparing the Study Files (TMF, ISF, Pharmacy Archive).
Management of the insurance policies of the studies that require it.
Monitoring tasks with the project manager.
Registration and periodic maintenance at national and international bases.
Responsible for complying with the metrics established by the Clinical Trials Unit.
Perform other tasks as required by the Clinical Trials Unit.
1.To have Spanish nationality, that of a member country of the European Union or to be a foreigner with residence and work permit in Spain.
2. Be in minimum possession of a Bachelor's Degree or Degree (with a Master's Degree) in Health Sciences or Administration. In the case of qualifications obtained abroad, their approval must be accredited or be in a position to obtain it.
Strict compliance with the requirements will be a necessary condition for the admission of candidates to the selection process.
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