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Senior Cra
hace 1 semana
- Madrid, Spain
- Permanent
Overview:
This is a fantastic opportunity to join a Mid-sized but rapidly growing Madrid Based CRO, with sites and operations across the Europe, this organisation is having a period of great success and looking to really grow into a powerhouse CRO within the EU and US.
Skills/requirements:
Minimum of 3 years experience as a CRA
Come from a background of Biotech's/Pharmaceuticals/CRO.
A relevant degree or equivalent.
Experience in submission and regulatory affairs (preferred)
A strong understanding of Clinical trials.
Main Duties:
- Performing site selection, initiation, monitoring and closeout visits,
- Maintaining all documentation relating to study setup and monitoring activities e.g. monitoring plans, visit reports, study status trackers
- Communicating regularly with assigned study sites and the project team
- Provide protocol and related study training to allocated sites
- Assess the quality of site practices, procedures and study data and escalating any quality issues as appropriate
- Employment Type: Fulltime, Home and Office based_
- Location: Madrid, Spain. (Hybrid/Remote)_
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