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I R C M

Research Assistant

Montreal, QC, Canada

Full-time · Temporary

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Applications open in a new tab.

Job details

Job type: Full-time · Temporary
Working hours: 35 hours/week
Posting language: English
Posted: Oct 6, 2026

Original job description

About the IRCM

The Montreal Clinical Research Institute (IRCM) is a world-class biomedical research center that puts science to work for health. The work of our teams contributes to major advances in research. We provide an environment where scientific rigor and collaboration drive the advancement of knowledge.

What you’ll love

Contribute to work that has a tangible impact on health and research.
Thrive in a rigorous, collaborative, and supportive environment.
Take part in challenging projects and continuous improvement initiatives.

Job Overview

We are seeking a Research Assistant with strong expertise in oligonucleotide synthesis, purification and quality control to support the development of the RNA Therapeutics Platform within the Sidney Altman Hub at the Montreal Clinical Research Institute (IRCM). The successful candidate will play a key role in establishing and operating oligonucleotide bioproduction and analytical capabilities for ASOs, siRNAs and sgRNAs. They will also help develop the platform’s therapeutic RNA and lipid nanoparticle activities in a highly collaborative environment, working closely with researchers, users and other team members.

Responsibilities

Contribute to establishing and operating the RNA Therapeutics Platform in collaboration with the platform lead.
Perform chemical synthesis of therapeutic and research oligonucleotides, including ASOs, siRNAs, sgRNAs and other formats, using automated synthesis equipment, including solid phase synthesizers.
Perform oligonucleotide purification, desalting, lyophilization, quantification and characterization.
Conduct oligonucleotide quality control using analytical approaches such as HPLC, LC-MS, UV spectrophotometry and other relevant methods.
Assist with the maintenance, optimization and troubleshooting of oligonucleotide synthesis and analytical equipment.
Contribute to the development, optimization and standardization of synthesis, purification and quality-control protocols.
Maintain rigorous documentation of activities in accordance with applicable quality procedures.
Contribute to in vitro RNA synthesis, purification and quality-control activities.
Participate in lipid nanoparticle (LNP) formulation and characterization according to platform needs.
Support the implementation and maintenance of the platform’s quality-management systems.
Work with researchers and platform users to understand their needs, advise on experimental approaches and follow up on projects.
Contribute to the development of new services and the continuous improvement of platform processes and activities.
Participate actively in team meetings, knowledge sharing and continuous improvement of platform services and procedures.
Establish and maintain effective, collaborative working relationships with platform users and team members, and help deliver high-quality scientific services.

What You Bring to the Table

Essential Requirements

Master’s degree (M.Sc.) in chemistry, biochemistry, molecular biology, biotechnology or a related field.
Hands-on experience in chemical oligonucleotide synthesis.
Experience in oligonucleotide purification and quality control.
Experience with automated oligonucleotide synthesis equipment, such as Shasta, MerMade, Dr Oligo or equivalent.
Experience with analytical techniques such as HPLC, LC-MS, capillary electrophoresis or similar methods.
Knowledge of RNA synthesis and analytical methods is an asset.
Experience in lipid nanoparticle (LNP) formulation is an asset.
Knowledge of molecular biology and biochemistry, including PCR, cloning, electrophoresis, nucleic acid quantification and western blotting.

Desired Skills

Excellent understanding of oligonucleotide chemistry and chemical modifications of nucleic acids.
Good knowledge of RNA biology and the mechanisms of action of therapeutic oligonucleotides.
Good understanding of quality-control principles applied to nucleic acids.
Ability to analyze and interpret complex analytical results.
Scientific rigour and excellent ability to document experimental activities.
Strong organizational skills and ability to manage multiple projects simultaneously.
Ability to work in a collaborative technology-platform environment.
Familiarity with laboratory information management systems (LIMS) and quality systems is an asset.
Knowledge of GMP/GLP is an asset.
Excellent teamwork skills in a multidisciplinary environment bringing together expertise in chemistry, biochemistry, molecular biology and RNA therapeutics.
Ability to communicate effectively with collaborators from varied backgrounds and contribute to a positive, engaging work environment.

Key Information

Schedule: Full-time (35 hours/week)
Position type: Temporary, 3-year contract

Benefits

20 days of vacation after one year.
10 personal or sick days.
Additional time off during the holiday season.
Defined benefit pension plan (RREGOP).
Group insurance plan.
Telemedicine services for you and your family.
Employee Assistance Program (EAP).
Bicycle facilities, including secure bike parking and showers.
Convenient location in the heart of Montréal.

Submit Your Application

Submit your application (resume) by clicking “Apply”.

To learn more about the IRCM: https://www.ircm.qc.ca

Selection Process

Selected candidates will be contacted for an interview. Background checks may be conducted depending on the nature of the position.

The IRCM values diversity, equity, and inclusion. We encourage applications from people of all backgrounds.

Accommodations may be provided upon request at any stage of the recruitment process. To request accommodations, please indicate this in the “Is there anything else you'd like to tell us about yourself?” section of the application form.

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More about this job

Responsibilities

The Research Assistant will establish and operate the RNA Therapeutics Platform, performing chemical synthesis, purification, and quality control of oligonucleotides. They will also collaborate with researchers to support lipid nanoparticle formulation and maintain laboratory equipment and quality management systems.

Requirements

Candidates must hold a Master's degree in chemistry, biochemistry, molecular biology, or a related field. Hands-on experience with automated oligonucleotide synthesis equipment and analytical techniques like HPLC and LC-MS is required.

Skills

Oligonucleotide synthesis
Purification
Quality control
HPLC
LC-MS
Automated synthesis equipment
Molecular biology
Biochemistry
RNA therapeutics
Lyophilization
Spectrophotometry
Troubleshooting
Documentation
Data analysis

Benefits

Vacation
Personal days
Sick days
Holiday season time off
Defined benefit pension plan
Group insurance plan
Telemedicine services
Employee assistance program
Bicycle facilities

Visa sponsorship

Not detected in the job text

Keywords

Oligonucleotide synthesis
RNA Therapeutics
Biomedical research
ASOs
siRNAs
sgRNAs
HPLC
LC-MS
Lipid nanoparticle
Solid phase synthesizers
Quality control
Molecular biology
Biochemistry
Biotechnology
Laboratory equipment
Protocol development
LIMS
GMP
GLP
Analytical chemistry

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