Clinical Research Project Assistant, Department of Critical Care Medicine

at  SickKids

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 Department of Critical Care Medicine is seeking a Clinical Research Project Assistant 1.0 fte to work closely with the clinical research coordinators, Project manager and/or P.I. to assist in study operations. This position includes many of the basic tasks of the clinical research process, such as entering data, maintaining of documents etc.

• Work collaboratively with research team members.
• Assists in the preparation of Research Ethics Board applications.
• Maintenance of regulatory documents including the development and upkeep of study binders (electronic/paper).
• Assists Project Manager with regulatory requirements (obtaining signatures, maintaining study trackers, collecting CVs, Medical Licenses & Training documents, organizing meetings, booking rooms).
• Assist with advance preparation for audits and site visits.
• Check data for accuracy and completeness; score data; enter data, including data re-entry; data cleaning
• Provide support to other research team members, where necessary.
• Assist with site training for site coordinators.
• Develop other study documents as required.
• Participate in study-related meetings