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 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.
What you’ll need to succeed
DEC or combination of pertinent experience and education.
1 year of equivalent experience an asset.
Knowledge of Good Clinical Practices.
Bilingualism is required (French and English).
Experience in clinical research environment and/or good knowledge of clinical trials; methodology and terminology will be considered as an asset.
Excellent organizational and prioritizing skills.
Good Communication skills.
Altasciences strives to provide a French working environment for its employees in Quebec. Although as part of its francization program has taken all reasonable steps to avoid imposing the above-mentioned requirement. Fluency in English is an essential requirement for the position of Quality Control Associate including, but not limited to, for the following reasons:
The requirement to have study protocols, designs and clinical research documents written and documented in English as required by industry regulatory agencies.
What we offer:
On site position at our Montreal office (1100 Beaumont); accessible by public transportation (Metro L'Acadie) and free parking lot for employees.
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
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MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH
Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!
Top Skills
What We Do
Outsourcing made easy with a one-stop solution to early-phase drug development.
We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering.
We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication.
Helping sponsors get better drugs to the people who need them, faster, for over 25 years.
Our full-service offering is always tailored to your specific research needs:
- Preclinical research
- Clinical pharmacology
- Drug formulation
- Manufacturing and analytical services
- Bioanalysis
- Program management
- Medical writing
- Biostatics
- Data management
- And so much more!
