Planning, coordinating, executing, auditing and result analysis of clinical and pre-clinical studiesAssisting relevant VP in diversified tasks in the areas of Quality assurance, Clinical and Regulatory affairs.

Independently plan, schedule and conduct:Non clinical site audit; Audits of GLP documents in support of a non-clinical study; Study based audits at a GLP/GCLP Laboratory for GLP and other regulated studies; Facility prequalification/qualification audits at Contract Research Organizations (CROs).Issue QA Audit Reports for the different auditsParticipate in SOPs, work instructions, forms and templates development and reviewReview and approve non-clinical parts of regulatory submissions (e.g. INDs, Ms).Asist in and provide GLP training programs.Asist in providing support in the preparation for and during a non-clinical site regulatory inspections

Senior study director in preclinical research. Manager of the large animal unit and in charge of ophthalmic research

Manager of preclinical trials in various fields of medicine including cardio-vascular, ophthalmic, dermatologic research and others