Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
1A
150 Altasciences Clinical Kansas Inc
Clinical Quality Control Associate II
Career Insights for Quality Assurance Manager
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Kansas data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Quality Assurance Manager focuses on prevention of mistakes and defects in manufacturing products. Develops procedures to ensure that quality standards are maintained. Manages all steps related to quality assurance as part of the quality management strategy of a company. May involve leadership of a team of quality assurance supervisors, specialists, and other associated staff members.
$110,311 / year median in Kansas
+2% projected growth
Job Description
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, detail oriented, well organized, customer service focused, able to work in fast-paced environment.