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/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.
What You’ll Need to Succeed
DEC completed in a related field.
Related work experience preferred.
Experience with eSource systems preferred.
Excellent communications skills in both French and English.
Able to multi-task, prioritize.
Excellent organizational skills.
Strong attention to detail.
Proven ability to work as part of a team in a very fast paced, deadline-driven environment.
Strong MS Office skills including Word, Excel, PowerPoint and Outlook and familiarity with HRMS systems.
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/Data Entry 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
Full time permanent position
37.5 hours a week;
On site position (1200 Beaumont ( In front of Metro L' Acadie and free parking for employees))
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
#LI-JG1
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!
