- Active participation in Clinical Study Teams.- Follow up on site selection and Ethics submission by the CRO.- Follow up on Insurance policy and certification accordingly to the clinical trial requirements.- Participation in selection and management of external CROs and other external providers for phase I to phase III respiratory studies (central laboratory, centralized ECG, spirometry and patient diary providers).- Ensuring quality on monitoring activities by the CRAs at the CRO.- Performing monitoring site visits for ensuring the quality of the sites and the performance of the CRAs.- Indeep quality revision on the eTMF/papaer TMFs for final filling.- Active participation in preparation of internal audits and site audits.- Active participation in a Mock Inspection for a MAA respiratory program in EU (November 2013).- Training for internal and external users on IMPACT (i.e: CTMS) and also on the Document Management System used in Almirall.- Preparation of project update Newsletters, etc.

As a MTC trainee in Almirall, I had the opportunity to gain a multidisciplinary knowledge of the main goals and challenges of any clinical development plan, working with different professional teams (Data Management, Drug Safety, Quality Assurance, Regulatory, Statistics, Study Information, etc.).