Salary Range: $88,990-$127,923/year. The starting salary for this position would be determined with consideration of the successful candidate’s relevant education and experience, and would be in alignment with the provincial compensation reference plan. Salary will be prorated accordingly for part time roles.

 

 

Join Our Collaborative Team as a Genomic Specialist

 

We are looking to hire 3 Genomic Specialists for our team!

 

Are you ready to revolutionize patient care and drive groundbreaking advancements in clinical genomics? The Cancer Genetics and Genomics Lab (CGL) at PHSA invites you to join our dynamic team as a Genomic Specialist, where your work will shape the future of cancer diagnostics and treatment across British Columbia. As a collaborative team of lab scientists, clinical genetics technologists, and dedicated support staff, our mission is to advance cancer diagnostics through cutting-edge genomic testing, ranging from single-gene analyses to next-generation sequencing panels. By joining us, you’ll contribute to life-changing advancements in patient care and work alongside an exceptional team of professionals who share your passion for excellence.

 

Our innovative environment leverages state-of-the-art technology to push boundaries and redefine possibilities. We prioritize career development through test development, research, and a culture of continuous learning. Our team’s impactful work aims to enhance diagnoses and provide patients with tailored therapeutic options through personalized medicine. Together, we foster a collaborative culture that celebrates multidisciplinary teamwork and shared achievements in advancing cancer care.

 

Our commitment to revolutionizing cancer care inspires us to deliver meaningful outcomes for patients. Joining the CGL team means being part of a transformative initiative that uses genomic innovation to shape the future of medicine. This is your opportunity to make a lasting impact—apply now and be part of something extraordinary.

 

Accountabilities

• Analyze and interpret complex genomic variants to provide critical diagnostic insights.
• Manage variant databases by adding, updating, and reviewing entries in alignment with the latest clinical guidelines.
• Draft and present genetic variant interpretation reports with precision and clarity.
• Leverage advanced genomic analysis tools, bioinformatics software, and public databases for cutting-edge data generation and interpretation.
• Contribute to the development of innovative diagnostic assays and the optimization of genomics workflows.
• Collaborate with interdisciplinary teams, including lab scientists, technologists, and operational leaders, to deliver high-quality patient care.

Qualifications

• A Master’s degree in Medical Genomics, Molecular Biology, Bioinformatics, or a related field, plus 3+ years of experience in clinical genomics or a similar setting.

• Relatable experience includes working as: Clinical Genomics Analyst, Genome/Genomics Analyst, Genomics Research Scientist and Genetic Laboratory Scientist.
• Expertise in sequence data analysis, variant prioritization/classification, and computational pipelines.
• Proficiency in bioinformatics tools, database management, and modern programming languages.
• Strong critical thinking, analytical, and organizational skills.
• Exceptional communication abilities and a collaborative mindset.

If you are a Clinical Genomics Analyst, Genomics Research Scientist, Genetic Laboratory Scientist, or have a related background, this role offers an unparalleled opportunity to grow, innovate, and make a lasting impact.

Join us in shaping the future of genomic medicine. Apply now and be part of something extraordinary.

 

** Please note: Support for nomination with the BC Provincial Nominee Program is not a guarantee, entitlement, nor an employee benefit after receiving a full time job offer with PHSA **