Operational Data Steward - Remote in Canada Job at Charles River Laboratories, Senneville, QC

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Job Description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.


IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.


Job Summary


As an operational data steward for our team, you will be responsible for implementing data use policies as determined by enterprise data governance initiatives, acting as a liaison between digital, Global Technology, DOT, Corporate Data Analytics and other similar departments/teams and business operations for all security assessment sites. This position is 100% remote.


In this role, primary responsibilities include:


  • Ensure that data-centric operational activities are aligned and leverage applicable data standards, governance processes, and overall best practices.
  • Assist data owners in the implementation and maintenance of consistency of CRL's critical operational data standards.
  • Participate on various projects and initiatives that impact operational activities to ensure that any data related changes and dependencies are identified, communicated and managed to ensure adherence with DOT established standards.
  • Identify gaps in data standard adherence and work with data owners to define, review, and remediate.
  • Integrate activities with those of other major organizational units (e.g. segments, departments, functions).
  • Assist global teams on initiatives to drive consistent use of data
  • Performs all other duties as assigned.

Key Elements


We are looking for the following minimum qualifications for this role:


  • Education: Bachelor’s degree (B.A./B.S.) or equivalent
  • Experience: 4 or more years related experience in scientific data presentation and/or scheduling.
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
  • Strong working knowledge of data stewardship. Ability to work independently and as a member of an integrated global team. Must be detail oriented with excellent organizational and communication skills. Ability to interact with all levels of staff. Ability to perform under pressure in a fast-paced, multi-task, deadline-oriented environment. Familiar with appropriate regulations, guidelines and guidance for the conduct of preclinical studies in North America and Europe.

Why Charles River ?


  • Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage)
  • Paid development training
  • Employee and family assistance program
  • Access to a doctor and various health professionals (telemedicine)
  • Vacation & Personal day policy
  • Many social activities

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us, THIS IS YOUR MOMENT!


IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

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