Clinical Research Project Coordinator

2 weeks ago

Toronto, Canada SickKids Full time

**About SickKids**:
Dedicated exclusively to children and their families, The Hospital for Sick Children (SickKids) is one of the largest and most respected paediatric healthcare centres in the world. As innovators in child health, we lead and partner to improve the health of children through the integration of healthcare, leading-edge research and education. Our reputation would not have been built - nor could it be maintained - without the skills, knowledge and experience of the extraordinary people who come to work here every day. SickKids is committed to ongoing learning and development, and features a caring and supportive work environment that combines exceptionally high standards of practice.

When you join SickKids, you become part of our community. We share a commitment and determination to fulfill our vision of _Healthier Children. A Better World_.

Don’t miss out on the opportunity to work alongside the world’s best in paediatric healthcare.

**Position Description**:
**Job Summary**:
The Clinical Research Project Coordinator (CRPC) will work closely with the research team in the _i_OUCH Pain Lab at The Hospital for Sick Children to assist with the protocol, data coordination, and data analysis of various randomized controlled trials. The Clinical Research Project Coordinator reports to the Principal Investigator or their designate (i.e., Project Manager).

**Project Summary**:
Through evidence-based research and knowledge translation processes, the _i_OUCH 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 CRPC will work closely with the PI or their designate with protocol and database planning, development, coordination and analysis for research studies within the _i_OUCH Lab.

**Specific job duties include**:

- Study set-up, including obtaining and maintain research ethics approval, research ethics amendments
- Participate in study recruitment, consenting, participant follow-up, and data collection.
- Responsible for study coordination across all participating sites.
- Oversee and participate in data management (e.g., data cleaning and data entry) and quantitative/qualitative data analysis.
- Working closely with the PI or their designate to oversee various randomized controlled trials within the program of research.
- Prepare study protocols with other study team members, ensuring correct research methodologies are applied.
- Design study databases (e.g. REDCap, Excel).
- In multi-centre trials, assist with staff training, and monitoring of standardized procedures across multiple sites.
- 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.
- Participate in other administrative activities to ensure the smooth running of projects.

**Here’s what you need**:

- Graduate degree in epidemiology or biostatistics, or equivalent experience.
- Minimum of three-years experience in clinical research.
- The ability to conceptualize the project goals into standardized data management practices.
- Excellent organizational skills and proficiency using quantitative statistical software, Stata or R preferred.
- Experience with qualitative software (i.e. NVivo) an asset. Experience in a pediatric clinical research is an asset.
- 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.

**Employment Type**: 1 year, 1.0 FTE Temporary contract

**Our Commitment to Diversity**:
The children and families we care for are from a variety of communities, and so are our employees. We welcome and encourage everyone to join our organization and be part of our team.

Thank you for your interest in joining SickKids. Only those applicants selected for an interview will be contacted. In accordance with our Hospital policy, employment at SickKids is conditional upon the Hospital’s receipt of all necessary documentation.

**How to Apply

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