LIMS Logistics Specialist

Planet Technology; Laval; On-site; USD 60,000 - 70,000; Full time

Job summary

An established industry player is seeking a dedicated LIMS Logistics Specialist to join their team. In this full-time role, you will leverage your expertise in Clinical Research and LIMS to coordinate study designs and support internal and external activities. Your contributions will be vital in ensuring compliance with GLPs and GCPs while providing training and resolving issues related to study designs. This innovative firm offers competitive compensation, benefits, and a supportive work environment where your skills will make a significant impact on advancing research initiatives. If you are passionate about science and eager to contribute to meaningful projects, this opportunity is for you.

Benefits

Competitive PTO

Group RRSP with employer match

Health benefits

Qualifications

• 2+ years in Clinical Research with experience in LIMS and regulated environments.
• Strong understanding of Study Protocols and Clinical Trials phases.

Responsibilities

• Coordinate study designs and support users of Watson LIMS.
• Perform sample reconciliation and manage discrepancies related to sample reception.
• Write and edit SOPs while ensuring compliance with GLPs and GCPs.

Skills

LIMS

Sample Management

Ligand Binding Assays

Mass Spectrometry

Understanding Study Protocols

Clinical Research

Writing SOPs

Education

BSc. in Life Sciences

Tools

Watson LIMS

Job description

This range is provided by Planet Technology. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$60,000.00/yr - $70,000.00/yr

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, Sample Management, 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 Sample Management, 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.
• Supporting study design creation and employee training for other sites.
• Creating and verifying Watson LIMS study designs based upon study protocols.
• Investigating and resolving issues related to study designs.
• Performing sample associations based upon sponsor manifests.
• Contributing to study design assessment meetings.
• 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.
• Participating regularly within process improvement initiatives.
• Working closely with QC reviews and Sample Management teams.
• Writing and editing SOPs as needed and conducting all work in compliance with SOPs as well as GLPs and GCPs.
• Ability to troubleshoot LIMS sample processing.

Seniority level

Associate

Employment type

Full-time

Job function

Science

Industries

Research Services and Biotechnology Research