Job Description

About SickKids

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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

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The Clinical Research Project Coordinator (CRPC) coordinates clinical research studies according to regulatory and institutional guidelines and requirements. This includes coordinating patient recruitment and data collection, study administration, preparing consents and paperwork required by the Research Ethics Board and organizing data entry and analysis. The CRPC also assists in the preparation of study results, including presentations, progress reports, and manuscripts.


Specific to this position, you will be coordinating projects that focus on pediatric plastic surgery and patient-reported outcomes in children and young adults with cleft lip and/or palate.

Here's What You'll Get To Do

Assist the Principal Investigator (PI) in new research proposals and preparation of grant applications; contributing to preparation of reports, presentations, and manuscripts Read and have a general knowledge of protocol and study measures Assist in design of case-report forms and/or questionnaires Assist P.I. with science review process Keep abreast of regulations and policies governing clinical research Develop informed consent documents based on regulations, REB consent templates and institutional requirements. Submit to REB and coordinate revisions. Assist collaborating sites with REB applications. Assist P.I. with annual approval process and amend protocols and consents as required Develop study binders for clinical department and study team use Encourage and foster collaborative relationships with the healthcare team at SickKids, other participating centres and government and community agencies Participate in audits, site visits and monitoring by SickKids and other regulatory bodies or industry sponsors Conduct literature reviews and keep current with study literature Assist with database design. Ensure the quality of the database and supervise database cleaning. Perform/assist with data entry and analysis including planning Participate or give in-services on study requirements Attend relevant departmental meetings or rounds in order to increase knowledge and understanding Assist with design/development of promotional materials/newsletters Develop and monitor timelines for study Provide information and documentation for potential protocol patients (consents, patient eligibility items, required pre-study testing and roadmaps) Confirm eligibility of and registering patients Initiate and maintain a research chart that will include original consent, patient protocol documentation, general correspondence, and case report forms Monitor serious adverse events or reactions and report immediately to PI. Following-up on adverse events including filing reports with internal and external regulatory bodies, notification of collaborators and/or patients Perform patient interviews and assessments as required by study protocols Maintain research equipment Provide feedback to patients/healthcare team and arrange clinical follow-up as required Organize materials to facilitate protocol adherence, including study binders and checklists of eligibility Co-supervise (with PI) Clinical Research Assistants, trainees, volunteers at SickKids and provide guidance for research staff at collaborating sites Assist in training/orientation of new research staff Prepare/submit purchase requisitions and invoices Maintain budget records

Here's What You'll Need

Bachelor of Science Certification as a clinical research associate (e.g., SOCRA, ACRP accreditation) is preferred 3-5 years related clinical research experience Ability to function independently yet collaboratively within a team Effective communication, interpersonal, facilitation and organizational skills A commitment to understanding and aiding in the pursuit of equity, diversity and inclusion objectives

Employment Type:

This position is for a 2-year contract with potential for renewal Hybrid work option may be possible depending on the phase of study


#LI-DNI

Our Commitment to Diversity

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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

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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

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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 into

ONE

document of 20 pages or less as you cannot upload multiple documents as part of your application.