Juan Valdez Email and Phone Number

Accountable for delivering the committed part of all clinical studies under their supervision according to agreed resources, budget and timelines complying with company Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations.To be responsible for co-ordinating the implementation of global and local Clinical Development processes, Clinical Procedural Documents, Quality & Compliance Manual documents.To ensure that Local Procedural Documents are compliant with global Procedural Documents, applicable international guidelines such as ICH/GCP as well as relevant local regulations.To provide advice and training on Clinical Development processes, Clinical Procedural Documents, applicable Quality & Compliance Manual documents, international Good Clinical Practice standards and local regulations to all relevant MC employees and external collaborators.To plan Quality Control activities and to perform them in collaboration with line managers