Clinical Research Project Coordinator-RI

The Hospital for Sick Children; Toronto; On-site; CAD 75,000 - 95,000; Full time

Job summary

The Hospital for Sick Children is seeking a Clinical Research Project Coordinator-RI to support pediatric research efforts. This role involves coordinating clinical trials and ensuring compliance with ethical standards. Candidates should have a strong background in clinical research, effective communication skills, and a commitment to improving child health.

Benefits

Employee benefits coverage including health, dental, and life insurance.

Focus on employee wellness.

Commitment to equity, diversity, and inclusion.

Qualifications

• 3-5 years related clinical research experience preferred.
• Certification as a clinical research associate is an asset.
• Experience developing and submitting REB applications.

Responsibilities

• Coordinate clinical research studies and manage patient recruitment.
• Develop informed consent documents and submit to REB.
• Conduct literature reviews and data analysis.

Skills

Effective communication

Interpersonal skills

Organizational skills

Education

Bachelor of Science or Medical Sciences undergraduate degree

Job description

Clinical Research Project Coordinator-RI

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Clinical Research Project Coordinator-RI

Join to apply for the Clinical Research Project Coordinator-RI role at The Hospital for Sick Children

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.

Reporting to the Labatt Family Heart Centre Research Manager, the Clinical Research Project coordinator works closely with the Heart Centre Principal Investigators (PI) to coordinate clinical research studies. This includes coordinating patient recruitment and data collection, preparing consents and paperwork required by the Research Ethics Board (REB), working on Health Canada Regulated Studies and overall study administration.

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
• 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
• 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
• 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
• 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
• 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
• Consult with Pharmacy regarding medication or placebo development and dispensing
• Prepare/submit purchase requisitions and invoices
• Maintain budget records
  
  

Here's What You'll Need

• Bachelor of Science or Medical Sciences undergraduate degree
• Certification as a clinical research associate (e.g., SOCRA, ACRP accreditation) is an asset (Or interest in working towards this certification)
• 3-5 years related clinical research experience preferred
• Previous experience developing and submitting REB applications, including addressing REB queries on initial study applications and amendments through to approval
• Previous experience working on Health Canada Regulated drug and/or device studies considered an asset
• 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 & inclusion
  
  

Here's What You'll Love

• This position is eligible for employee benefits coverage including but not limited to; health, dental and life insurance. The full benefits package will be discussed at the time of offer.
• A focus on employee wellness with our new Staff Health and Well-being Strategy. Self-care helps us support others.
• A hospital that welcomes and focuses on Equity, Diversity, and Inclusion.
• The opportunity to make an impact. Regardless of your role or professional interest, you will be making a difference at SickKids and contributing to our vision of Healthier Children. A Better World.
• For more on why you'll love working at SickKids, visit our careers site.
  
  

Employment Type

• Temporary full time
• 1.00FTE
• Year + 1 day contract
  
  

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.

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.

Technical difficulties? Email [e-mail] 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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management and Information Technology

• Industries

  Hospitals and Health Care

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