Mohammed Izaz Email and Phone Number

Over 10 years of experience in the field of Clinical Research Monitoring in the therapeutic area of Diabetes, Endocrinology, Psychiatry, nephrology and Oncology (Biologic s/Biosimilars) and Vaccine studies.Perform site selection, initiation, monitoring and close out visits in accordance with contracted scope of work and GCP. Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, electronic case report form (eCRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. Provide assistance and Technical Expertise to more less experienced clinical staff and Mentoring during accompanied site visit.  Ensure Compliance to SOPs Assist in developing and implementing new techniques in monitoring activities Assist in preparing sites for audits and contribute to resolve findings. Provide training in Operational techniques & SOPs  Day to day communication with central or local laboratories, and other providers/vendors.  Liaise with central laboratory on project management/protocol issues Training site staff on study related aspect and GCP (Worked with 3 GCP/Clinical Trial naive sites) Organize and coordinate Investigators’ meeting  Maintain regulatory documents/Trial Master Files Reconciliation and Management of clinical trial supplies Managing payments to the sites and vendors.