Quality Control Associate at Altasciences
Montréal, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

30 Oct, 25

Salary

0.0

Posted On

30 Jul, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

English, Regulatory Agencies, Working Environment

Industry

Pharmaceuticals

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 Quality Control Associate is responsible for reviewing and validating data collected during the screening phase of participant selection for clinical trials. This role ensures that all data complies with the study protocol, Good Clinical Practice (GCP) guidelines, and Standard Operating Procedures (SOPs).

WHAT YOU’LL DO HERE:

  • Performing live quality control (QC) of all data collected as part of screening and to ensure compliance to the study specific protocols and SOPs.
  • Ensuring all corrections to raw data and derived data are completed.
  • Identifying error trends and report them to management.
  • Printing laboratory results and update participant files.
  • Calling participants to schedule appointments.
  • Performing blood verification between Clinical Research Organizations.
  • Answering QA reports, data management queries, generate report deviations when necessary.
  • Prepare study binders.
Loading...