Quality Control Associate II

Posted 7 Days Ago
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Overland Park, KS
In-Office
Entry level
Information Technology • Analytics • Biotech
The Role
The Quality Control Associate II ensures quality control in clinical trials, maintains data confidentiality, and assists in audits while mentoring team members.
Summary Generated by Built In

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 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. The Clinical Quality Control Associate II will conduct What You'll Do Here 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.

What You’ll Need to Succeed

  • High School Diploma or GED and related work experience required; college degree and related work experience preferred.

  • Good Communication skills

  • Detail oriented, well organized, customer service focused, able to work in fast-paced environment.

#LI-AN1

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

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The Company
HQ: Laval, Quebec
1,832 Employees
Year Founded: 1995

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!

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