Job Summary:
The Clinical Research Data Analyst will work closely with the research team in the iOUCH Pain Lab at The Hospital for Sick Children to assist with data management, analysis, and reporting of various sources including results of randomized controlled trials, and national registries. The Clinical Research Data Analyst reports to the Principal Investigator or their designate (i.e., Project Manager).
Project Summary:
Through evidence-based research and knowledge translation processes, the iOUCH Lab at The Hospital for Sick Children aims to improve the lives of children and adolescents through the use of innovative information and communication technologies.
Here's What you get to do:
The Data Analyst will work closely with the PI or their designate with database planning, development, management, and analysis for research studies within the iOUCH Lab.
Specific job duties include:
- Working closely with the PI or their designate to conduct statistical analyses for multiple clinical research studies within the lab
- Collaborate with other study team members, to develop analysis plans, ensuring correct research methodologies are applied.
- Design, build, and maintain study databases (e.g. REDCap, Excel) to support ongoing and future research projects.
- Lead the design, build, and implementation of a REDCap-based national, multisite registry
- Establish and document data management workflows, data dictionaries, and/or SOPs
- Develop and implement data validation, cleaning, monitoring and auditing procedures
- Develop programming to produce regular study progress reports.
- Conduct regular data quality audits and data cleaning.
- Conduct data analysis of clinical trials with supervision from a Senior Statistician.
- Clearly communicate and interpret study results to research team members.
- Assist with abstract, poster, and manuscript preparation.
Here's What you need:
- Graduate degree in epidemiology or biostatistics, or equivalent experience.
- Minimum of three-years experience in clinical research.
- Previous clinical trial experience is required, including application of quantitative research methodology.
- The ability to conceptualize the project goals into standardized data management practices.
- Advanced proficiency in REDCap preferred.
- Excellent organizational skills and proficiency using quantitative statistical software, Stata or R preferred.
- High precision and attention to detail, patience and ability to work with complex tasks
- Superior communication, organization and time management skills.
- Ability to develop strong working relationships.
- A commitment to understanding and aiding in the pursuit of equity, diversity and inclusion objectives.
Employment Type: 1 year, 1.0 FTE Temporary contract
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