- High School Diploma or GED and related work experience required;
- College degree an asset;
- Bilingualism (French and English);
- Detail oriented;
- Well organized;
- Customer service focused;
- Able to work in fast-paced environment.
- Permanent Full-Time position (37,5 hours/week);
- Day shift.
- On site position (Montreal office)
- Must be available to work 1 every 3 weekend.
- Health/Dental/Vision Insurance Plans
- RRSP with Employer Match
- Paid Vacation and Holidays
- Paid Sick and Bereavement Leave
- Training & Development Programs
- Employee Referral Bonus MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
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Clinical Quality Control Associate II - Mont-Royal, Canada - Altasciences
Description
Clinical Quality Control Associate II
1200 Beaumont Ave, Montreal, QC H3N 1W5, Canada Req #4669 Wednesday, May 15, 2024 Your New Company
At Altasciences we allmove 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 Clinical Quality Control Associate II is responsible for the quality control (QC) review of clinical trial data and working with the Quality Systems team to complete QC related tasks. He will conduct tasks performed within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs).
What you'll do here
• Ensure the confidentiality of clinical trial participants and sponsors is respected;
• Maintain and advocate a high level of quality and customer service within the department;
• Act as a mentor and coach the Quality Systems team members;
• Record, track and ensure the resolution of data queries;
• Assist in sponsor/regulatory audits;
• May document and/or report clinical trial related deviations (i.e. SOP, protocol);
• Identify and track error trends, report trends that may require re-training;
• Compile data and maintain computerized files and/or update deviation tracking systems;
• Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events;
• Proactively communicate issues and/or problem resolutions to departmental supervisors and managers;
• Complete and/or maintain training as required per jobs needs;
• May provide departmental supervisors/managers with feedback for performance reviews;
• Perform general administrative tasks when required;
• Other tasks as assigned by management.
What you need to succeed
What we offer
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
