Are you ready to join an exciting and dynamic team at our Preclinical Site near Colombia, MO? As an Associate Quality Control Coordinator, you'll play a crucial role in upholding the highest standards of quality and precision in our research operations. If you're passionate about ensuring the integrity of scientific data, maintaining meticulous records, and contributing to cutting-edge research, this is the perfect opportunity for you.

What You'll Do Here

At our Preclinical Site, we are committed to excellence in every aspect of our work. As a Quality Control Associate, your primary responsibility will be to guarantee that all study and facility data align with our stringent SRC Standard Operating Procedures (SOPs), the study protocol, and Good Laboratory Procedure (GLP) requirements. Your daily tasks will include:

• Staying Ahead: Maintaining a high level of competency in SRC Standard Operating Procedures (SOPs), GLP regulations, and ALCOA+ standards, ensuring we are always at the forefront of industry best practices.
• Protocol Perfection: Reviewing draft protocols before pre-study meetings and meticulously scrutinizing the final protocol for all studies prior to data collection, ensuring the foundation is rock-solid.
• Getting It Right from the Start: Preparing for study initiation by actively participating in pre-study meetings, setting the stage for precision from the outset.
• Data Guardianship: Conducting daily 100% second-party reviews of all study and facility data, including Pristima edits and back-entries, leaving no room for error.
• Data Vigilance: Vigilantly monitoring data corrections suggested by our Report Services and Quality Assurance teams to ensure that all corrections to raw data are accurately reflected in the study data.
• Quality Gatekeeper: Daily tracking of data recording errors during data review and participating in data quality assessments of Operational staff, upholding the highest standards.
• Schedule Adherence: Reviewing final study schedules and daily schedules to ensure strict adherence to protocol requirements, ensuring consistency throughout the study.
• Timely Delivery: Monitoring the study timeline and ensuring that study data is well-prepared for Data Hand-off, including the resolution of any data errors that may arise.
• Meticulous Organization: Maintaining study binders and facility record binders to guarantee proper filing and easy access to critical information.
• Collaborative Excellence: Working closely with Supervisors, Study Directors, Report Coordinators, and Quality Assurance teams to address any data clarity issues promptly, fostering a collaborative and innovative work environment.

What You’ll Need to Succeed

To thrive in this role and contribute to our mission of excellence, you should possess:

• A high school diploma or GED and at least 1 year of relevant experience; alternatively, a Bachelor’s Degree and no previous experience will be considered, or an equivalent combination of education and experience.
• Proficiency in Microsoft Office applications (Word, Excel, Outlook) to efficiently handle data and communication tasks.
• Prior experience in record-keeping or detailed note-taking, showcasing your attention to detail and meticulous organizational skills.

Join us in this exciting journey of scientific discovery, where precision and quality are paramount, and your contributions make a significant impact. If you're ready to take your career to the next level, apply now and be a part of a team that's pushing the boundaries of scientific excellence.

What We Offer

Benefits 

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
• E mployee Referral Bonus Program
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