Study Design Specialist, Watson LIMS at Altasciences
Laval, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

22 Nov, 25

Salary

0.0

Posted On

23 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

English, Regulatory Agencies

Industry

Hospital/Health Care

Description

YOUR NEW COMPANY!

At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you’re a recent college graduate or seeking your next career opportunity, it’s time to discover your future at Altasciences.
We are better together and together We Are Altasciences.

Responsibilities

ABOUT THE ROLE

The Study Design Specialist, Watson LIMS main responsibility is to review Study Protocols/Plans and create study design in Watson LIMS to ensure study samples can be inventoried and analyzed.

WHAT YOU’LL DO HERE

  • Create and verify study designs in Watson LIMS based on study protocols
  • Perform sample associations based on sponsor manifest
  • Support other sites by creating study designs
  • Manage discrepancies related to sample reception
  • Write memo to file and ensure execution
  • Generate reports as requested
  • Supports sample management with the preparation of clinical sample kits
  • Facilitate study designs for data reporting
  • May perform sample reconciliation
  • May provide training to new employees as needed
  • Participate in process improvement initiatives
  • Work closely with QC reviewers and Sample Management teams to address issues
  • To conduct all work in compliance with SOPs, GLPs, GCPs and observe all company guidelines and policies.
  • Perform any other tasks as required by management
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