Rahmat Umar Email & Phone Number

Calgary, AB, CA

Mississauga, Ontario, Canada

• Participate in study start-up activities by gathering requirements, authoring key module documents, and assisting with module configuration and validation of databases for pharmaceutical Phase I to III multicenter.
• Initiate and review Data Management Plans, data export specifications, and data transfer agreements for various studies
• Address data collection, inventory, and quality issues encountered at trial sites or sponsor level and appropriately escalate to the company leadership
• Maintain study drug accountability and reconciliation from the start-up of trials to close-out
• Communicates information on applicable RTSM project activities to stakeholders, including internal and sponsor study teams
• Prepare, review, and approve site and support materials as well as helpdesk documentation

Ontario, Canada

• Assisted module design, configuration, and validation for different studies by completing functionality scripts – testing data capture
• Contributed to the quality and accuracy of clinical study reports by creating the specifications and validating the reports
• Reviewed study documentation, including the protocol, project timelines, CTM expiry memos, and study notes to file
• Wrote study-specific memoranda, central email communications, and other study-specificcommunications

North York

Mississauga

• Conducted outbound calls to existing customers regarding their energy bills
• Addressed and resolved customer issues via telephone calls, utilizing effective listening and problem-solving skills

• Interviewed, collected, and recorded health-related data in paper-based medical records
• Trained medical staff on the developed standard operating procedures to improve hospital efficiency
• Ensured implementation of the treatment plan through communication with other involved healthcare providers and conducting regular ward rounds

• Ensured timely and adequate documentation of procedures
• Monitored subjects for immediate adverse events and recorded them appropriately in paper CRFs
• Attended continued medical education to remain current on regulatory requirements and healthcare standards

• Transcribed recorded patient interviews into medical records
• Collaborated with co-investigators on both internal and nationwide research projects
• Extracted and abstracted patient data from medical records to create datasets for analysis
• Received training on and adhered to workplace guidelines, policies, and bylaws

Kwara, Nigeria

• Collaborated with a group of healthcare professionals to formulate and administer questionnaires to study participants for the collection of health-related data
• Conducted a literature review and presented research findings on the public health-related topic, "Pattern of disabilities in a residential school for the handicapped in Ilorin, Nigeria"

College Graduate Certificate, Clinical Research

Certificate Of Completion, Conducting Research Responsibly, Global Health

Certificate Of Completion, Leadership And Management In Health, Public Health

Bachelor Of Medicine, Bachelor Of Surgery (M.B.B.S.), Medicine