Quality Control Coordinator

Posted 8 Hours Ago
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Columbia, MO, USA
In-Office
Entry level
Information Technology • Analytics • Biotech
The Role
The Quality Control Coordinator ensures study and facility data are compliant with SOPs and GLP regulations, reviews protocols, maintains data quality, and communicates with team members to improve processes.
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 primary responsibility of the Quality Control Coordinator is to ensure all study and facility data is in accordance with SRC Standard Operating Procedures (SOP's), the study protocol, and Good Laboratory Procedure (GLP) requirements.

What You’ll Do Here:

  • Maintain competency in the current SRC Standard Operating Procedures (SOPs), GLP regulations, and ALCOA+.

  • Reviews protocols and study schedules for all studies prior to data collection. Suggests areas of improvement to the protocol or Pristima schedule, as needed.

  • Maintains high data quality standards and performs 100% second party review daily on all study and facility data, including Pristima edits and back-entries. Brings forward suggestions to correct any findings.

  • Assists with data corrections suggested by Report Services and Quality Assurance to ensure all corrections to raw data are reflected accurately in the study data.

  • Track data recording errors daily during data review and participate in data quality assessments of Operational staff.

  • Review final study schedules and daily schedules to ensure conformity of protocol requirements. Monitor the study timeline and ensure study data is prepared for Data Hand-off, including resolution of data errors.

  • Maintains high standards toward organization and follows through with communications, as well as following up on findings.

  • Proposes improvements/refinements in data review capabilities and develops different data review methods to improve efficiency.

  • Communicates effectively and professionally with outside departments, management, and other employees. Motivates and mentors team members.

  • Work closely with Supervisors, Study Directors, Report Coordinators, and Quality Assurance to resolve data clarity issues.

What You’ll Need to Succeed:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION and/or EXPERIENCE: High school diploma or GED and 1 year of relevant experience; Bachelor’s Degree and no previous experience; or an equivalent amount of education and experience.

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:

  • Health/Dental/Vision Insurance Plans

  • 401(k)/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 Review 

#LI-TA1

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!

Skills Required

  • High school diploma or GED and 1 year of relevant experience
  • Bachelor's Degree
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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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