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Altasciences

Integrated CRO for early-phase drug development

Associate Scientist - Flow Cytometry

Regulatory & Quality (Life Sciences)Posted on Nov 13
Full-timeLaval, QC, CanadaNo salary listedIn-person

About the Job

Requirements

  • Ideally have a college degree and/or university degree in Chemistry, Biochemistry, Immunology, or an applicable field.
  • Have experience in regulated clinical and/or preclinical studies; typically, three years of experience is preferred.
  • Know regulatory agency guidelines, understand general Standard Operating Procedures, and have good knowledge of Good Laboratory Practice regulations.
  • Be able to read and understand study plans and protocols.
  • Be able to coach and mentor people.
  • Communicate well both in writing and verbally in French and English.
  • Deeply understand general Standard Operating Procedures and have excellent knowledge of Good Clinical Practice and Good Laboratory Practice regulations.

Responsibilities

  • Tabulate and perform final data batch reviews, including multi-batch trend analysis, and complete required study documentation, including approving Memo to File or SOP, protocol, or study-plan deviations where appropriate.
  • Provide reports and/or final results within study timelines, ensure deviations, exceptions, and events are appropriately reflected, and ensure all analyses are reported accurately.
  • Assist in writing validation and analytical plans and reports, and provide comments and/or recommendations as needed for the bioanalytical portions of preclinical and clinical protocols, study plans, laboratory manuals, Data Transfer Agreements, and other documents.
  • Assist with planning sample analysis by maintaining timelines and scheduling commitments.
  • When assigned, order reagents and materials and verify inventory. Perform literature searches and draft work plans for assay development as assigned.
  • Assist with risk and costing evaluations. Based on training and competency, perform laboratory bench work for method development or validation, interpret results, document and tabulate data, and troubleshoot when required.
  • Keep the BPI and/or Senior Scientist involved through ongoing communications.
  • Write, review, and update method Standard Operating Procedures as needed; support responses to Quality Assurance reports; and complete management-assigned studies and tasks based on scientific competency and training, which may include method development, validation, or sample analysis projects.
  • Provide feedback on progress and assist in sponsor teleconferences as required.
  • Conduct all work in compliance with applicable Standard Operating Procedures, Good Clinical Practices, Good Laboratory Practices, company guidelines, and policies.
  • Observe health and safety standards regarding personal protection, laboratory maintenance, and work procedures.

Desired Qualifications

  • Experience in regulated clinical and/or preclinical studies, typically three years, is preferred.

About the Company

Altasciences

Integrated CRO for early-phase drug development

Altasciences provides integrated early-stage drug development services, covering preclinical testing, early clinical trials, and contract manufacturing. It functions as a single, in-house CRO that coordinates discovery support, safety testing, clinical research, and manufacturing to streamline a program from start to early proof of concept. The company differentiates itself by offering an end-to-end, one-stop path rather than requiring clients to contract multiple vendors. Its goal is to help innovator programs move quickly and efficiently through early development to speed up decision making and progression to later-stage trials.

Company size
1,001-5,000
Company stage
Early VC
Total funding
$6.7M
Headquarters
Laval, Canada
Founded
1976

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