Lambda Canada | Careers
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Careers

Delivering the best is accomplished through hiring the best. They are the pillars that hold up every quality promise that we make. That’s why we at Lambda are always looking for qualified and energetic individuals, with a desire for excellence, to join our team.

 

The Lambda Family as we call it is also a closely knit group sharing not just professional, but personal bonds through various cultural activities and celebrations right through the year.

 

Lambda Therapeutic Research Inc. welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.

 

You can apply for the opportunities that you may be qualified for to
jobs@lambdacanada-cro.com,listing your desired position in the subject line.

 

Notice to Agencies:
Lambda Canada has established agency relationships whereby we only work with Preferred Suppliers. We are not currently enlisting new suppliers, but should you like to email us your contact information you may do so by sending it to jobs@lambdacanada-cro.com. Lambda Canada does not accept unsolicited resumes submitted directly to any employee via email or fax, unless there is a valid written and signed agreement in place for that position. If there is no such agreement, Lambda will not be liable to pay any fee with respect to the individual or resume regardless of whether Lambda hires the individual concerned

Current Opening(s)

Sample Custodian Assistant

KEY RESPONSIBILITIES:         

  • Developing, executing, and maintaining a highly organized, structured, and controlled system for sample storage.
  • Ensuring the Freezer room is clean and organized.
  • Receive samples from Lambda and outside clinic sites. Follow up to track shipments that are not received when expected.
  • Inspect and reconcile samples upon receipt. Resolve any discrepancies between shipment records and physical sample inspection.

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QC Data Reviewer

KEY RESPONSIBILITIES:        

  • Review study files after completion and ensure that they are accurate and legible according to Protocol, SOPs and Regulations
  • Ensure all prepared study source documents and/or Forms are in accordance to protocols and SOPs
  • Perform live QC during the conduct of studies including sample bundling and shipping process
  • Review all hard copy source data and Biznet electronic source data related to all protocol and SOP driven parameters

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Senior Research Scientist / Research Scientist

KEY RESPONSIBILITIES:       

  • Developing and support validation of bio-analytical methods under GLP and SOP guidelines.
  •  Assisting the lab management in evaluating external bio-analytical methods and working with external laboratories on collaborative projects.
  • Following up on the recent progress and development in the area of biopharmaceutical sciences, specially in drug analysis/instrumentation and providing lab management (or other related departments) with suggestions on the future development of the analytical laboratory.
  • Working with Senior Scientists

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Clinical Research Coordinator Assistant

KEY RESPONSIBILITIES:      

  • Assist the CRC on monitoring and tracking the progress and execution of each study to ensure compliance with client timelines, study Protocol, SOPs, GCP guidelines and applicable regulations.
  • Review of assigned protocols, eCRF and other protocol documentation for accuracy and feasibility
  • Work with CRCs and other members of the study teams to ensure study performance meets or exceeds client expectations
  • Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data

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Clinical Research Coordinator (CRC)

KEY RESPONSIBILITIES:      

  • Assist the CRC on monitoring and tracking the progress and execution of each study to ensure compliance with client timelines, study Protocol, SOPs, GCP guidelines and applicable regulations.
  • Review of assigned protocols, eCRF and other protocol documentation for accuracy and feasibility
  • Work with CRCs and other members of the study teams to ensure study performance meets or exceeds client expectations
  • Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data

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Lambda Benefits Plan

Lambda is committed to providing its Team Members with a competitive compensation and benefits program, that when coupled with the potential for positive career progression, provides an environment where committed and motivated individuals can excel.

 

Our comprehensive benefits package is company funded and includes:

  • Dental Care
  • Visioncare
  • Extended Healthcare
  • Short-term and Long-Term Disability
  • Life-Insurance
  • Global Travel Insurance

 

We also have a voluntary Retirement Savings Program with a Company matching program to help our Team Members plan for their future.