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**:
The Clinical Research Project Coordinator 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 conducting data analysis (qualitative and quantitative). The CRPC also assists in the preparation of study results, including presentations, progress reports, posters, and manuscripts.

The Clinical Research Project Coordinator will work closely with the Principal Investigator and Clinical Research Project Manager to assist in all study-related activities.

To read more about the research done in this lab, check out the following links:
**Here's What You'll Get To Do**:

- Contribute 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 questionnaire
- 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.
- Conduct literature reviews and keep current with study literature.
- Assist with database design, in conjunction with Principal Investigator and Database Analyst. Ensure the quality of the database and supervise database cleaning. Perform/assist with data entry and analysis, including planning.
- Attend relevant departmental meetings or rounds in order to increase knowledge and understanding.
- Develop and monitor timelines for study.
- 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.
- Perform patient interviews, assessments as required by study protocols.
- Maintain research equipment.
- Provide feedback to patients/healthcare team and arrange clinical follow-up as required. May include writing clinical reports.

**Here’s What You’ll Need**:

- A Master's degree in Epidemiology, Health Science or a related field with a minimum of three years experience in clinical research. Post-secondary degree in a health-related discipline (e.g., Nursing, Epidemiology, Health Sciences, Psychology) with 2 years related clinical research experience. A clinical professional degree may be an asset, as would certification as a clinical research associate (e.g., SOCRA, ACRP accreditation).
- Exceptional written and verbal communication skills
- Experience writing research proposals, preparing presentations, and managing research projects
- Demonstrated organizational and problem-solving skills
- Demonstrated ability to be self-motivated and self-directed
- Excellent computer skills (strong knowledge of Microsoft Word, Excel, PowerPoint, and data collection platforms such as REDCap)
- Ability to work independently and within a team
- Ability to work in a fast paced environment and meet deadlines
- Ability to pay close attention to detail while maintaining view of the larger scope

**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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