Screening Quality Control Associate

at  Altasciences

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.
About the role
The Screening Quality Control Associate will perform the quality control of data collected during the screening phase of a clinical trial. The Screening Quality Control Associate will execute all and ensure all data is in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.

What you’ll do here:

• Performing the 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.

What you’ll need to succeed

• DEC or combination of pertinent experience and education.
• At least 1 year of equivalent experience.
• Experience in clinical research environment and/or good knowledge of clinical trials; methodology and terminology will be considered as an asset.
• Knowledge of Good Clinical Practices.
• Bilingualism is required (French and English).
• Excellent organizational and prioritizing skills.
• Good Communication skills.

What we offer:

• On site position at our Montreal office (1100 Beaumont)
• Candidates must be available between 9am and 7pm.
• Flexibility to work overtime when necessary.
• Usually one Saturday out of two (sometimes on Sundays).

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences’ Benefits Package Includes:

• Health/Dental/Vision Insurance Plans
• RRSP with Employer Match
• Paid Vacation and Holidays
• Paid Sick and Bereavement Leave
• Employee Assistance & Telehealth Programs

Altasciences’ Incentive Programs Include:

• Training & Development Programs
• Employee Referral Bonus Program
• Annual Performance Reviews

• Performing the 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