Screening Quality Control/Data Entry Associate at Altasciences
Montréal, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

09 Dec, 25

Salary

0.0

Posted On

10 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

English, Working Environment, Regulatory Agencies

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/Data Entry Associate is responsible for the review of screening source documents and other related documents used to capture data during the screening evaluation and data entry of clinical data within an Electronic Data Capture (EDC) system.

WHAT YOU’LL DO HERE

  • Performs internal review and UAT of source used to capture data during Screening. Maintain tracking tools to ensure review of screening CRF and data entry milestones are met.
  • Generate Delegation of Authority log and Protocol Training Report and other documents related for Screening.
  • Create/Review/Update Screening Information and ICF Discussion Reference Sheet and other documents related.
  • Creates, maintains Screening and Enrollment Log for all studies.
  • Performs data entry of clinical trial data into electronic data capture (EDC) software in compliance with protocol/SOP and EDC guidelines.
  • Identify error trends and report trending to departmental management.
  • Record, track and ensure the resolution of data queries in timely manner.
  • Act as a resource and provide support when necessary
  • Maintain and advocate a high level of quality and customer service within the department.
  • Ensure the confidentiality of clinical trial volunteers and sponsors is respected.
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