Education and qualification: Degree in biology, biochemistry, medicine or nursing.
Knowledge and professional experience:2 years or more. Study coordinator and data management in clinical trials.
Tasks: Recruiting, inclusion/exclusion criteria, informed consent, protocols, data strict manipulation, contact with the patient, data acquisition and collection and storage of samples for further analysis and all the involving protocols.
Number of available positions: 1
Full-time position (40h/week)
Starting date: 31/05/2021
Length of the contract: 1 year extendable
Workplace: Unitat de Recerca Clínica Oncològica
Applicants should submit a full Curriculum Vitae and a cover letter with the reference IC16_21 to the following email addresses: curriculum@iispv.cat before May 25th 2021.
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