Research Director

Medical Affairs &Clinical Research Manager.

Site Monitoring Managment , GCP training of the study staff , Manageing all the following activities (Site evaluation , investigator selection, Site initiation , Staff training on protocol , electronic CRF , IVRS Randomization system and helping in resolving medical queries, tracking of IP, accountability of study drug and logistic requirements at custom and site logistic arrangements of biological samples sending outside Saudi Arabia , preparations for the audit, assisting sites in Data Queries resolution, site close out and archiving , Medical and Research training of the staff in Hospitals - MOH - CRO - Pharmacutical companies) .

Main activities/responsibilities:Ensure overall implementation of ClinServ within territory and liaise with all required infrastructure. Overall clinical operation team activities supervision, guarantee of quality and milestone target. Responsible of units activities, Plan and implement all aspects of clinical studies.Interacts with BD and Operations of ClinServ, Beirut to determine the most proactive and realistic projects milestones and targets. Coordination of administrative activities involved in the operations function for clinical development.•Supervise and monitor clinical trials to ensure absolute adherence to Good Clinical Practice in accordance with ICH-GCP standards, Declaration of Helsinki, Federal Regulatory Requirements and study procedures .

Managing the Clincal trial held in Egypt & GCC country ,Attending all the site activities , Regulatory Activities and Country Clinical research activities .

Acting as a Project Manager for the Regional Projects R&D. Conducting site evaluation and performing feasibility studies. Conducting study initiation visits. Reviewing the submission package of Ethics Committees. Validation and verification of CRF data against source documentation. Collection of CRFs and supporting of site staff in resolution of queries. Verification and notification about any Serious Adverse Events. Verification of protocol compliance, detection and notification of protocol deviation fro the medical point of view. Maintenance of site files. Vertification of adequate records of subject idenitification,

Managing All the project activities and research regulatory activity on site in KSA .

Managing all the medical and research activities related to the marketed products .

Dubai and Kuwait. Managing the teams for sales, marketing and medical for promotion of a variety of brands. Conducting Phase IV studies.Feb 2005 ­ May 2007 Field Medical Manager .

Main activities/responsibilities: Managing all sales and marketing business activities and leading sales and marketing team of five business associates and product specialists. Responsible for the annual business planning, sales and budget forecast, key account management, distribution team management and customer services. Conducting medical / training conferences and PMS studies of XOLAIR.

Managing all the marketing activities and medical training of the assigned products .

Main activities/responsibilities: Promotion and sales of whole RX portfolio in South Area of KSA. Conducting PMS studies.

Main activities/responsibilities: Responsible for Cardiovascular brand promotion in Giza and Cairo. Conduction of PMS studies conducted in

Managing All the patients’ medical conditions and minor operations , delivery and family planning .