##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 ofHealthier Children. A Better World.

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

##Position Description

**Clinical Research Project Coordinator Assistant,**CALIPER Program - Pediatric Laboratory Medicine

About the CALIPER Program

The**CALIPER (Canadian Laboratory Initiative on Pediatric Reference Intervals)**program is an internationally recognized research initiative dedicated to establishing comprehensive pediatric reference intervals for clinical laboratory tests. These reference intervals are essential for accurate interpretation of laboratory results and improved diagnosis and monitoring of disease in children and adolescents.

Since its inception, CALIPER has generated one of the world's largest pediatric reference interval databases and has significantly influenced laboratory medicine practice globally.

The program continues to expand through innovative research studies, international collaborations, and development of digital clinical tools.

More information:
www.caliperproject.ca

Position Overview

The CALIPER program is seeking a highly motivated**Clinical Research Project Coordinator Assistant (CRPCA)**to support the coordination and execution of CALIPER research studies and associated projects.

Working closely with theProgram Head and multidisciplinary research team, the CRPA will play a central role inclinical research administration, regulatory compliance, and study documentation, while also contributing to participant recruitment, laboratory activities, and data management.

This position is ideal for candidates with strong experience inclinical research coordination and regulatory processes, and offers the opportunity to contribute to impactful pediatric research in a leading academic environment.

Here's What You'll Get To Do:

Clinical Research Administration & Regulatory Compliance (Primary Responsibility)

• Lead and manage all aspects ofresearch study administration and regulatory documentation
• Prepare, review, and submitResearch Ethics Board (REB) applications, amendments, and renewals
• Develop, maintain, and ensure compliance withstudy protocols, Standard Operating Procedures (SOPs), and regulatory documents
• Ensure adherence toinstitutional policies, Good Clinical Practice (GCP), and regulatory requirements
• OverseeREDCap database design, data entry, and quality assurance processes
• Maintain accurate and secureparticipant records and study documentation
• Coordinate study audits, monitoring activities, and regulatory inspections
• Track study progress, timelines, and reporting requirements
• Liaise with internal stakeholders, external collaborators, and industry partners
• Record and circulate meeting minutes and maintain study communication records

Community Engagement & Participant Recruitment

• Plan and implement recruitment strategies across theGreater Toronto Area (GTA)
• Establish partnerships with community organizations including schools, pediatric clinics, community centres, and daycare centres
• Develop recruitment materials and outreach strategies
• Deliver presentations to community stakeholders and participants
• Coordinate and manage community clinic days
• Monitor participant safety and report adverse events to the Principal Investigator

Research Coordination & Team Support

• Coordinate day-to-day research study operations and timelines
• Recruit, train, and supervise volunteers and student trainees
• Assist with hiring and supervision of research staff
• Coordinate scheduling of staff (e.g., phlebotomists) for clinic days

Laboratory Support

• Perform laboratory procedures including sample processing and storage
• Support reference interval studies and validation experiments
• Maintain laboratory equipment and sample inventory
• Prepare and ship biological samples for analysis

Data Management & Scientific Activities

• Maintain and update the CALIPER database and mobile application
• Perform statistical analyses and assist with data interpretation
• Contribute to manuscripts, abstracts, and scientific presentations

Here's What You'll Need:

Education

-BSc or MScin health sciences, biomedical sciences, public health, or a related field required

Certification

-Certified Clinical Research Coordinator (CCRC) designation required

Experience

• Strong experience inclinical research administration, regulatory processes, and REB submissions
• Experience inclinical research coordination or project management
• Experience incommunity outreach and participant recruitmentpreferred
• Experience working withchildren and families

Skills

• Excellent written and verbal communication skills
• Strong organizational and project management abilities
• Strong understanding ofGCP and regulatory requirements
• Experience withREDCap or similar research databases
• Familiarity with statistical software (e.g., R, SPSS)
• High attention to detail and ability to manage multiple priorities
• Strong leadership and teamwork skills

Additional Requirements

• Ability to travel within the Greater Toronto Area
• Commitment to institutional policies and procedures

Employment Type: Full-time 12 months contract, renewable annually up to five years (subject to funding and performance)

Why Join CALIPER?

• Work within aglobally recognized pediatric laboratory medicine program
• Gain experience inclinical research leadership and regulatory coordination
• Contribute tohigh-impact publications and international collaborations
• Engage in meaningfulcommunity-based pediatric health research

#LI-DNI

##Our Commitment to Diversity

SickKids is committed to championing equity, diversity and inclusion in all that we do, fostering an intentionally inclusive and culturally safe environment that reflects the diversity of the patients, families and communities we serve. Learn more about workplace inclusion.

##Accessibility & Accommodation

If you require accommodation during the application process, please reach out to our aSKHR team. SickKids can provide access and inclusion supports to eligible candidates to support their full engagement during the interview and selection process as well as to ensure candidates are able to perform their duties once successfully hired. If you are invited for an interview and require accommodation, please let us know at the time of your invitation to interview. Information received related to access, inclusion or accommodation will be addressed confidentially.

##How To Apply

Technical difficulties? Email ask.hr@sickkids.ca with a short description of the issues you are experiencing. We will not accept resumes sent to this inbox but we are happy to respond to requests for technical assistance.

Tip:Combine your cover letter and resume intoONEdocument of 20 pages or less as you cannot upload multiple documents as part of your application.

Every application is reviewed by a human recruiter and all hiring decisions are made by people. In some cases, AI-assisted tools are used to help review applications based on job-related qualifications.

All positions posted on the SickKids Hospital's Careers Site represent current vacancies, unless otherwise posted in the job description.