Moaz Afaqui

Ready to accept all kinds of challenging and responsible jobs in the area of Pharmacy where I can serve my competency and render my role through reputational aspects of pharmacy and able to meet & matches the ambitions of the organization.

• Certification of participation in international conference on the theme of "RECENT QUALITY RESEARCH ON HERBAL FORMULATION", 9th and 10th march 2024.
• Certification of attending the national conference on "DRUG DISCOVERY IN PHARMACEUTICAL RESEARCH & ITS FUTURE PROSPECTIVES", 9th and 10th may 2024

• Coordinate, organize and maintain all documentation required by sponsor or CRO (source documentation, case report forms, study and regulatory binders, and patient binders).
• Prepare and process all institutional review board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments and adverse events reporting.
• Obtains the appropriate signatures for regulatory forms.
• Collect appropriate data using CRF source doc's
• Report AE/SAE according to sponsors/IRB requirements.
• Resolve data queries with sponsor and CROs.
• Recruit, screen and enroll potential study patients as specified per protocol.
• Participate in the conduct of audits by study sponsors, CROs, the FDA, and other entities as required.
• Schedule patient visits and any necessary testing.
• Process and ship blood, urine and serum specimens for each trail.
• Obtain records required to complete case report forms.
• Show vigilance in patient safety, protocol compliance, and data quality.

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