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Project Coordinator (Hybrid)

Charles River Laboratories International Inc (CRL)

Montreal (Senneville), Quebec, CA, H9X 3R3

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 a project coordinator  for our site located in Senneville, Qc., with opportunity to work from home. You will be responsible for determining project costs for different services/products. In coordinating with the sales team, finance and operations departments, contributing laboratories, suppliers, subcontractors and consultants to ensure accurate project tracking in financial systems to determine the cost of proposals and change orders. Monitor and update project milestones resulting in accurate revenue recognition and billing to clients. 

The following are the main responsibilities of the Project Coordinator position:

  • Responsible for development and maintenance of a study from initial inquiry notification to study completion.
  • Develop the suggested selling price (SSP) for potential new business by initiating and building the study costs utilizing templates in SAP.
  • Prepare, coordinate, and maintain critical milestone dates for execution of the study.  
  • Manage changes and cost adjustments in SAP as communicated by Client Services, Operations or as necessary for accurate costing.
  • Provide feedback/suggestions on template structure/content and necessary updates.
  • Assist in monitoring procedural metrics to determine accuracy and relevance to study type and operation processes. 
  • Make recommendations, and develop solutions for any roadblocks that would inhibit a milestone date being met (i.e., changes of work scope, material shipment delays, availability of study related inventory and equipment). 
  • Communicate changes per sponsor requests to affected departments with agreement from Client Services. Ensure any schedule impact is reported to Client Services in conjunction with scheduling/procurement personnel.
  • Verify with Client Services that cost changes have been communicated to the sponsor and approved.
  • Provide reports and metrics as needed.
  • Maintain and update databases and or other tools as required. 
  • Observe study related activities with the technical staff and become familiar with study related processes as needed. 
  • Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].

Key Elements

If you have the following qualifications, we will train you for the rest: 

  • Bachelor’s degree (B.A. /B.S.) or combination of education and experience may be accepted as a satisfactory substitute 
  • 1-2 years related experience in project management in a laboratory or research environment.
  • Working knowledge of SAP applications preferred. 
  • Ability to multi-task and to prioritize and re-evaluate priorities as situations change
  • Excellent written and verbal communication skills, organizational skills, and attention to detail. 
  • Working knowledge of computer software (MS Office, MS Project, Excel and database experience preferred)

Role Specific Information :

  • Location: Senneville  (Shuttle service from Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site), Free parking 
  • Salary: 45k 
  • Schedule: Weekday schedule, Monday to Friday 
  • Permanent position as of the hiring, full time 37.5hrs per week 
  • Perks: remote work, occasional  on site 

Why Charles River?

  • Competitive benefits upon hiring. We pay up to 85% of premiums (medical & dental coverage) 
  • Paid development training 
  • Employee and family assistance program 
  • 24/7 access to a doctor and various health care professionals (telemedicine) 
  • 3  weeks’ Vacation & 5  Personal day policy  
  • Numerous organized social activities.

If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team, IT'S YOUR TIME!

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. 

About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. 

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

Job posted: 2023-04-20

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