Quality Control Associate Role at CenExel USA
Looking for a rewarding quality control job in clinical research? CenExel is hiring a Quality Control Associate to ensure clinical trial documentation accuracy, compliance, and integrity. Be part of a team driving excellence in research across CNS and early phase studies.
Job Details:
- Job Category: QA / Data Regulatory
- Requisition Number: QUALI003843
- Location: CenExel iResearch, 250 E. Ponce de Leon Ave., Suite 800, Decatur, GA 30030, USA
- Employment Type: Full-Time
- Work Environment: Office and Clinic; Remote work possible
- Travel: Occasional travel for audits or training
About the Company:
CenExel is a nationwide clinical research site and patient network serving the life sciences industry. With 18 science-led Centers of Excellence, CenExel provides the right patients at the right time. Recently acquired by BayPine Capital Partners, the company delivers exceptional medical and scientific support for CNS and early phase studies. CenExel emphasizes teamwork, positive leadership, and work-life balance while offering competitive compensation and benefits. Explore more Quality control job offers.
Educational Requirements:
- Bachelor’s degree in life sciences, healthcare, or a related field (required)
- Advanced degree (preferred)
- 1–3 years clinical research experience, including 1 year in QC, QA, or documentation review
- Certification in clinical research (e.g., ACRP, SOCRA) is a plus
Key Responsibilities of Quality Control Associate Role:
- Perform quality control job duties including reviewing trial documents (informed consent forms, case report forms, regulatory binders, monitoring visit reports) for accuracy and completeness
- Identify discrepancies, deviations, or data entry errors and coordinate with teams for resolution
- Support QC of Trial Master File (TMF) documents, paper or electronic
- Assist in internal audits and inspection readiness activities
- Collaborate with clinical operations, data management, and regulatory teams to maintain documentation standards
- Maintain QC metrics and support quality improvement initiatives
- Ensure compliance with GCP, ICH, FDA, EMA, and CenExel SOPs
Skills Required for Quality Control Associate Role:
- Strong attention to detail and organizational skills
- Excellent written and verbal communication
- Ability to work independently and in a team
- Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint)
- Familiarity with eTMF, EDC, and CTMS systems preferred
Benefits of the Quality Control Associate Role:
- Competitive salary and generous benefits package
- Health, Dental, Vision Insurance
- Life Insurance, LTD, STD
- 401k plan
- Positive and collaborative work environment
- Opportunities for career growth in clinical research
