Responsible for Resources and Allocations in Spain. Continuos checking of metrics and procedures for improvements. Responsible for the line management, recruitment and selection, training, coaching and performance management of designated Clinical Management staff. Develops and provides training on procedural documents and other processes relating to Clinical Management. Provides mentoring, work direction and coaching through activities such as co-monitoring visits, file reviews and visit report reviews. Conducts regular performance appraisals/reviews with direct reports and facilitates their professional development. Uses metrics and key performance indicators to manage individual and team performance. May lead the Clinical Management team for a country or geographic area, or may lead or contribute to initiatives that contribute to Clinical Development/PPD business objectives.Accompanier: Authorised to conduct PAVs (Performance Assessment Visits) to provide ongoing training, evaluation and development of the PPD monitor

Responsible for the line management, recruitment and selection, training, coaching and performance management of designated Clinical Management staff. Develops and provides training on procedural documents and other processes relating to Clinical Management. Provides mentoring, work direction and coaching through activities such as co-monitoring visits, file reviews and visit report reviews. Conducts regular performance appraisals/reviews with direct reports and facilitates their professional development. Uses metrics and key performance indicators to manage individual and team performance. May lead the Clinical Management team for a country or geographic area, or may lead or contribute to initiatives that contribute to Clinical Development/PPD business objectives.Accompanier: Authorised to conduct PAVs (Performance Assessment Visits) to provide ongoing training, evaluation and development of the PPD monitor

Coordinates Regulatory Compliance Review activities within Spain. Identifies mentors, assigns and advises RCR reviewers in the RCR process.Appropriately trained to perform a final and independent quality control of essential documents required to start and maintain a clinical trial

Acted as Lead CRA on several Clinical Trials. Reviewed reports and performed start-up activities, pre-study visits, site initiation visits, site monitoring visits and close-out visits. Present at investigator and CRAs meetings. Translation of several study documents. Coordination of monitors from many countries. Preparation and review of study templates.

Performed start-up activities, pre-study visits, initiation visits, monitoring visits, close-outs visits. Translation of different study documents. Performed query resolution activities and participated in an interim database locks and the final database lock. Also, performed archiving activities.