Experience

eDucate Health

• Canada
• E-learning
• 1 - 100 Employee

• Content Manager

  • Jul 2011 - Present

  Innovate R&D is an electronic-learning portal of medical information for healthcare professionals, patients, and caregivers - Write comprehensive peer reviewed articles; which bridges the growing gap between the abundance of online medical information and the healthcare provider’s need of immediate relevance to patient care It software vendor management, budgeting - Participate in medical & scientific exchanges with KOL's of medical/scientific community - Managed projects and assisted in webinar development



Institute for Clinical Evaluative Sciences (ICES)

• Canada
• Civic and Social Organizations
• 1 - 100 Employee

• Clinical Research Coordinator

  • Jul 2008 - Jul 2011

  • Assigned to work through a Regional Stroke Center (Trillium Health Center) • Trained to use a web-based encrypted data collection of Ontario Stroke Registry (OSR) system • Utilized EDC system for outsourcing the data collected from EMR in clinical sites • Outsourced and collected data from clinical sites for the internal database repository at Sunnybrook Hospital achieving almost 100% accuracy, meeting the timelines according to planned objectives • Delivered, prepared and distributed timely status reports • Conducted regular reviews and audits of data security, privacy and confidentiality as to ensure GCP and Ethics compliance contributing with suggestions and recommendations • Participated actively in ICES research projects addressed to influence the design, implementation and evaluation of health policies and the delivery of health care



Department of Neurology - Trillium Health Centre - Mississauga, ON

• Clinical Research Coordinator

  • Sep 2006 - Jul 2008

  • Collected, processed, and reviewed case report forms using EMR • Assisted with project planning and development for assigned clinical investigations Lead coordinator responsible for site initiation, recruitment, consents and mentoring • Literature Research including Drug profiles, FDA, ICH, and GCP regulations, guidelines, policies and practices for conducting clinical investigations. • Responsible for IRB/IEC submission and renewals • Experience with audits by authorities for accuracy and conduct of research projects • Responsible for reviewing source documents for data accuracy, that lead to publish articles in peer reviewed journals



Department of Oncology and Hematology - The Aga Khan University Hospital - Pakistan

• Clinical Research Associate

  • Sep 1996 - Nov 2005

  • Collected, processed, and reviewed case report forms • Review of source documents • Review of essential documents required by the regulatory authority inspection to determine if the trial is being conducted in accordance to guidelines, regulations, and the protocol. • Review of onsite documentation of adverse event forms • Responsible for monitoring and recruiting patient groups and fulfilling all the pre-requisites according to the protocols for different clinical trials. • Collected, processed, and reviewed case report forms • Review of source documents • Review of essential documents required by the regulatory authority inspection to determine if the trial is being conducted in accordance to guidelines, regulations, and the protocol. • Review of onsite documentation of adverse event forms • Responsible for monitoring and recruiting patient groups and fulfilling all the pre-requisites according to the protocols for different clinical trials.



Department of Medicine, Ziauddin Medical University. Pakistan

• Resident

  • Jan 1995 - Jan 1996

  On call resident medical officer (RMO) in internal medicine On call resident medical officer (RMO) in internal medicine



Department of Oncology and Hematology, Aga Khan University Hospital

• Clinical Research Assistant

  • Jan 1991 - Jan 1993

  • Data collection • Analyzing results • Participating and presenting scientific presentations • Data collection • Analyzing results • Participating and presenting scientific presentations