LIMS Logistics Specialist

2 weeks ago

Laval, Canada Planet Technology Full time

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

  • Primarily responsible for the coordination of study designs in support of internal/external activities within the organization.
  • Supporting all users of Watson LIMS and study design related issues/questions; users include Watson Designers, Study Director/BPI, Sample Manager Teams, and Clinical/Pre-Clinical Sites.
  • Performing sample reconciliation as needed.
  • Providing colleague training on study designs cross departmentally to include training documentation creation and updates, new employees on LIMS/study designs, and more.
  • Supporting study design creation and employee training for other sites.
  • Creating and verifying Watson LIMS study designs based upon study protocols, while coordinating design requests and assigning these to appropriate members.
  • Investigating and resolving issues related to study designs.
  • Performing sample associations based upon sponsor manifests.
  • Facilitating study designs for data reporting.
  • Contributing to study design assessment meetings to determine best approach in the creation of study protocols.
  • Managing discrepancies related to sample reception.
  • Authoring file memos, while ensuring proper execution.
  • Generating reports as required for various uses.
  • Working with IT department to solve problems as well as with IT validation teams to perform UAT and test Cases.
  • Participating regularly within process improvement initiatives.
  • Working closely with QC reviews and Sample Management teams, while also participating in SOP reviews and updates.
  • Writing and editing SOPs as needed and conducting all work in compliance with SOPs as well as GLPs and GCPs, while observing all organizational guidelines and policies.
  • Ability to troubleshoot LIMS sample processing through the understanding of how samples are logged into, tracked and then maintained within the system.

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