DIRECTOR
مجموع سنوات الخبرة :9 years, 11 أشهر
Office of Information and Documentation EU/LIBYA MOH
•Provides direct leadership and management for PHC research operations team members
•Continuously evaluates research program compliance, quality, and effectiveness, identifies, and develops opportunities for improvement that provide greater value for stakeholders
•Leads process improvement and organizational change initiatives toward program optimization
•Partners and collaborates with the PHC Compliance office to evaluate and address research compliance issues and risks
•Encourages expanded participation from existing physician investigators through action oriented and expert support and helps to inspire and support new investigators in the sponsored research program
•Organizes and structures PHC research administrative services to expand the capacity of the research program with a focus on increasing and diversifying sources of revenue and financial support
•Directs an effective system of marketing and communication across PHC, the research community, and key stakeholders, to build and promote a positive image of PHC sponsored researchd research.
•Directing and implementing Clinical research plans and programs according to established design principles. Directing the integration of the CDP and DDP
•Participation in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds
•Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication
•Leading the development of Clinical Protocols to meet CDP objectives
•Planning clinical trials (design, operational plans, settings) based on these clinical development strategies
•Developing of clinical development strategies for investigational or marketed Oncology drugs
•Evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications
for Alkhums teaching hospital and health institute office.
•Assist Senior Director, Clinical on developing of clinical program for projects
•Develop study specific training documents and investigator’s brochures
•Participate in the development of implementation of clinical trial documents
•Manage CRO’s and other vendors; monitoring and audit activities to ensure studies compliance with GCP/ICH guidelines
•Conduct monitoring and co-monitoring activities
•Maintain current knowledge of relevant regulations, including proposed and final rules
•Lead all necessary activities including setting up, monitoring and reporting of bio studies
courses: WHO Certificate In medical Registration And Coding (ICD-10)
EDUCATION