About Global IQ
Global IQ is a full-service clinical research organization (CRO) committed to empowering its clients with the knowledge and support to bring products and devices to market quickly and efficiently. Global IQ provides clients with customized services for Phase II-IV clinical studies ranging from initial strategic planning through to regulatory submission and approvals. Founded by an experienced clinical investigator, our client-focused team is comprised of trained clinical operations personnel including, project managers, clinical research associates (CRAs), other clinical support staff and data management experts. Other members of the team include computer experts and QARA personnel. Our employees have extensive clinical trial expertise and knowledge in a wide variety of therapeutic areas. Global IQ’s philosophy is to tailor each study team to provide the client with quality expertise, which combined with our proprietary Electronic Data Capture (EDC) system, offers both cost efficiency and timely, reliable data. We are a team of highly-skilled, experienced, and flexible individuals who are continuously trained and educated in clinical trials in order to provide exceptional customer experience.
Global IQ has full-service offices in both North and Latin America, and our proprietary EDC system is designed for rapid data collection and maintenance from sites worldwide. The Latin American office is strategically located in Buenos Aires, Argentina, and provides services to all of Latin America.. Global IQ is also part of the ResearchPoint Global Partnership with trial capabilities in Europe, Asia, South Africa and Australia.
Global IQ’s corporate headquarters are in Edmonton, Canada.
Some highlights of Global IQ and its approach are:
- Careful strategic trial planning prior to trial initiation
- Detailed strategic trial planning prior to trial initiation
- Identification and recruitment of dedicated, proficient, and knowledgeable investigators
- Utilization of international sites to select the most appropriate trial population for each study, resulting in both rapid patient recruitment and quality clinical data
- Customization of the study’s team according to expertise and previous experience, affording the client a dedicated and focused team with pre-eminent service
- Utilization of proprietary user-friendly EDC software and electronic systems in each trial that provide a central data warehouse, resulting in real-time data monitoring, timely adverse event reporting, and facilitation of rapid decision-making as the trial progresses
- Vigilant clinical monitoring by trained, highly-accessible professionals throughout the trial
- Experienced QARA personnel are available to assist with all regulatory submissions
- Consideration for the client’s needs maintained by constant communication and consultation throughout the trial
- Accountability for all aspects
of the trial.
Global Partnership
GlobalIQ is a member of Research Point Global - a partnership of small CROs which work together to have a global reach.