LIMS Logistics Specialist

LIMS Logistics Specialist – (Full-time) – Onsite – Quebec Canada

Contract Research Organization seeks a full-time onsite LIMS Logistics Specialist with 2+ years’ experience working within Clinical Research within a CRO. This person should have expertise in LIMS, and SampleManagement, Ligand Binding Assays, and / or Mass Spectrometry. Additionally, this individual should have a thorough understanding of Study Protocols and Plans from various phases of Clinical Trials (Phases I-IV) and Safety Assessment (ideally Preclinical Toxicology Studies). Lastly, experience and knowledge having worked within a GLP and GCP environment and writing SOPs are also required. Opportunity offers competitive base compensation based on individual expertise and seniority. Also offered are benefits, competitive PTO, and a Group RRSP with an employer match of 100% of individual contribution each pay period, up to 3% of annual salary.

REQUIREMENTS

• Canadian Citizenship or Work Permit.
• Location within Canada, ideally already local to Quebec.
• Ability to work full-time from organizational onsite location.
• Valid passport for US travel, as necessary.
• BSc. Or higher degree in Life Sciences or related area.
• Experience working for a CRO and within regulated environments to include FDA, GLP, GCP and TPD.
• 2+ years in Clinical Research with 1+ years exposure to LIMS.
• Experience with SampleManagement, Ligand Binding Assays and / or Mass Spectrometry.
• Ability to understand Study Protocols and Plans, and from various clinical trials phases (I-IV), and Safety Assessments (Pre-Clinical Toxicology Studies).
• Knowledge of concentrations storage and reporting.

RESPONSIBILITIES