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 (CRPC) 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 the provision of pediatric burn care, investigating novel therapies to treat burn wounds as well as improve burn scars, and establishing patient-reported outcome measures for the pediatric burn population.

**Here's What You¿ll Get To Do**:
**Protocol related**:

- Possess in-depth knowledge of study protocols and study measures.
- Assist in design of study protocols, data collection forms, and/or questionnaires.
- Assist PI 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 PI 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 data entry and analysis using REDCap.
- Attend relevant departmental meetings/rounds to increase knowledge and communicate new research projects.
- Assist with the supervision of medical and undergraduate student research projects.

**Research Subject Related**:

- Provide information and documentation for potential protocol patients (e.g., consents, patient eligibility items, required pre-study testing, roadmaps).
- Confirm eligibility of participants for research studies (e.g., confirm criteria for eligibility satisfied, signed consent available).
- Initiate and maintain research records that will include original consent, patient protocol documentation, general correspondence, and case report forms.
- Monitor serious adverse events or reactions, and immediately report them to the PI. 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 assessments and/or interviews 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 Science is required. SOCRA certification in conducting clinical research would be considered an asset.
- A minimum of two years of previous clinical research experience specifically in the field of burn care is required.
- Previous experience in writing manuscripts and delivering scientific presentations is required.
- Ability to perform multiple concurrent tasks with excellent project management skills.
- Ability to 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
- A commitment to understanding and aiding in the pursuit of equity, diversity and inclusion objectives

**Employment Type**: Full-time Temporary 1 Year Contract with Modified Benefits (i.e., health & dental).

**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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