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.

In support of the SickKids 2025 Strategy and the vision of Unprecedented Outcomes Powered by Precision Child Health (PCH), the Translational Genomics (TG) team is hiring a full-time Research Analyst (Genome Analyst, Genomicist, Research Genetic Counsellor) to join our dynamic research team. The successful applicant will be part of a multi-disciplinary team that applies genome sequencing and other novel genomic technologies for rare genetic disease research. We are looking for a Research Analyst with experience analyzing and interpreting genome data, who can balance multiple projects and work collaboratively to support the various initiatives of the TG team. This is a unique opportunity to use your scientific skills combined with leading edge technologies to advance research, improve patient care, and contribute to the advancement of genomic medicine.

Here's What You'll Get To Do

• Work with a team of physicians, scientists, genetic counsellors, bioinformaticians, and research coordinators to ensure the analysis of research genomic data from a variety of research projects.
• Analyze genome sequencing (short read and long read) and RNA sequencing data
• Interpret and classify genetic variants detected in patients and their relevance to human disease by reviewing data collected from internal and external databases as well as published literature
• Maintain complete and accurate documentation of data analyzed and supporting evidence and present findings to study teams
• Support the strategic priorities of Translational Genomics node and partake the development, implementation, and evaluation of ongoing and emerging initiatives
• Participate in the development of operating procedures and evaluation of new genomic technologies, with the possibility of contributing to academic activities by analyzing and preparing data for publication.
• Have a flexible work arrangement, with a combination of on-site and remote work.

Here's What You'll Need

• A M.Sc. or Ph.D. degree in Molecular Genetics or a related field with experience in genomic data analysis and interpretation for the purpose of rare disease diagnosis
• Keen interest in genomic research and desire for continuous learning
• Self-motivation to learn about new technologies, approaches, and tools to develop strategies that effectively respond to emerging needs and research interests
• Familiarity with genetic test technologies
• Experience with interpretation of genetic variants and variant interpretation guidelines, and proficiency in using relevant genomic databases, tools and resources for data analysis (e.g. USCS, gnomAD, DGV, ClinVar, DECIPHER, IGV, GTEx)
• Capacity to critically review medical/scientific literature and accurately impart and document findings
• Demonstrated ability to be a team player and work independently
• Proven ability to work resourcefully and prioritize tasks to effectively balance competing demands from multiple concurrent projects
• Excellent organization and time management skills
• Strong oral and written communication skills and professionalism
• Previous experience in a clinical or research laboratory setting is preferred
• A commitment to understanding and aiding in the pursuit of equity, diversity and inclusion objectives

Employment Type 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 ask.hr@sickkids.ca 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.