Clin. Res. Project Coord.-ri

3 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**:
The Clinical Research Project Coordinator works closely with the PI to coordinate clinical research studies according to regulatory and institutional guidelines and requirements. The PI’s research interests include: improving surgical outcomes in cleft and craniofacial surgery, improving surgeon performance by understanding the role emotions play in our judgement, decision-making, and attention, and improving access to surgical care in resource-limited settings. The position further 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 assist in the preparation of study results, including presentations, progress reports, and manuscripts. May also fulfill Clinical Research Assistant responsibilities. Job duties will include, but not be limited to:
**Here's what you’ll get to do**:

- Protocol related:

- Read and have a general knowledge of protocol and study measures.
- Assist in design of data collection 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 P.I. with annual approval process and amend protocols and consents as required.
- Assist with data management duties. Ensure the quality of the data collection process, 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.
- Research Subject Related:

- Provide information and documentation for potential protocol patients (consents, patient eligibility items, required pre-study testing, roadmaps).
- Confirm eligibility of patient (confirm criteria for eligibility satisfied, signed consent available) and register 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 Principal Investigator. Follow-up on adverse events according to SickKids' Policy. This includes filing reports with internal (REB), and external regulatory bodies' notification of collaborators, and/or patients.
- Perform patient interviews, assessments as required by study protocols.
- Organize materials to facilitate protocol adherence, including study binders and checklists of eligibility

**Here’s what you’ll need**:

- Master’s degree in sciences, social sciences or a health-related discipline is an asset, but not required.
- Previous clinical research assistant experience in both qualitative and quantitative studies is required.
- Function independently yet collaboratively within a team.
- Effective communication, interpersonal, facilitation and organizational skills.
- Strong computer skills (Microsoft Office, REDCap, Internet and MEDLINE searches).
- Effective communication, interpersonal, organizational and problem-solving skills.
- An interest in advancing their clinical or research career to ultimately benefit the lives of others.

**Employment Type**:

- 1 Year temporary contract. This position is a hybrid role.

**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.

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