Dailenis Gloria Laredo Rodriguez

• Participated in the pre-screening, recruitment of study subjects. Explanation of the study protocol to the subjects and obtaining Informed Consented. Received , stored , dispensed,collected and maintained the inventory of investigational product as per requirement of the protocol an GCP. Assisted with development and submission of the study documents(e.g.,IRB documents, Lab related documents) to the sponsor-representative and IRB. Interacted with monitors and internal auditors regarding the conduct of clinical trials. Excellent knowledge of GCP/ICH guidelines and procedures.

Analyze samples, such as blood, urine and tissue, to detect diseases or infections. Order, stock and distribute laboratory supplies. Use microscopes, automated cell counters, and others instruments to perform test. Follow safety guidelines, know emergency procedures and wear appropriate personal protective equipment.

·A Randomized double-blind, placebo-controlled, parallel,group,dose ranging study to assess the efficacy,safety and tolerability of subcutaneous XXX in adult participants with moderate to severe asthma.

·A 2-stage,Adaptive,Randomized,Double-blind , placebo-controlled, multicenter Study to evaluate dose and treatment effect of XXX compared with placebo in participants with Knew Osteoarthritis Pain.

·A Phase 3, Multicenter, Open label, Long Term trial Evaluating the long term Safety and Tolerability of Once Daily XXXX capsules in Children and adolescents with Attention Deficit/Hyperactivity Disorder.

·A phase 3, Double Blind, Randomized , Placebo controlled , Parallel Group , Multicenter Study of XXXX in subjects who have mild to moderated Alzheimer`s Disease.

·Multicenter Randomized, Double blind ,Placebo and Active-Controlled Trial to evaluated the efficacy of XXXX monotherapy for the treatment in Adolescents (13-17 years old) with Schizophrenia.