Quality Assurance Auditor, DMB

Celerion

Tempe, Arizona

JOB DETAILS
SKILLS
Artificial Intelligence (AI), Auditing, Biometrics, Clinical Medicine, Clinical Trial, Communication Skills, Conduct Studies, Contract Research Organization (CRO), Data Management, Detail Oriented, Document Management, Electronic Data Capture (EDC), GCP (Good Clinical Practices), Information Technology & Information Systems, Information Technology/Systems Audit, Laboratory, Multitasking, Operational Audit, Presentation/Verbal Skills, Quality Assurance, Quality Management, Regulations, Team Player, Time Management, Vendor/Supplier Evaluation, Willing to Travel, Writing Skills
LOCATION
Tempe, Arizona
POSTED
10 days ago
Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  

Are you looking for an opportunity to be involved in creating life-saving treatments? If so, we can't wait to meet you!
 
Celerion, a leading global contract research organization, seeks a Quality Assurance Auditor to support our rapidly growing Data Management and Biometrics department. The successful candidate will have Quality Assurance expertise within a GCP environment. This role will be located at either our Lincoln, NE or Tempe, AZ facilities.
 
Role: The role of the Quality Assurance Auditor is to assess and assure study, project and process compliance with protocols, Controlled documents, and applicable regulations and guidelines through audits.

Responsibilities:

  • Carry out auditing of study, project, and process reports, records and data; report audit findings to operations via QA audit reports; and determine acceptability of the responses and verify the corrections (includes but not limited to Clinical Study Report audits, Protocol audits and Electronic Database Capture (EDC) audits).
  • Interact with internal and external clients to discuss QA observations and study-related issues; and maintain effective and professional working relationships within and across departments in relation to study projects.
  • Participate and lead in the improvement initiatives intended to improve quality, compliance of study, project data and reports; effectiveness and efficiency of the processes.
  • Detect quality issues and the need for CAPAs and evaluate deviations 
  • Assist with the preparation for and hosting of client audits and/or regulatory inspections.
  • Participate in the preparation, conduct and follow-up for System Audits and Vendor Audits

Qualifications:

  • Bachelor’s degree in science, IT, business, or similar
  • 2-5 years of quality/laboratory/clinical experience
  • Excellent oral and written communication skills
  • Ability to organize and manage multiple priorities
  • Excellent time management skills
  • Attention to detail, tactful, and diplomatic
  • Proficiency in using electronic data and computerized systems.  
  • Ability to travel, as needed  
Celerion Values:       Integrity   Trust   Teamwork   Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

About the Company

C

Celerion

We Are Celerion

Our 40+ years of experience, innovative strategies, global capabilities, and expertise in early phase research make us faster than our competitors. That means you get key data sooner, enabling you to make earlier go/no-go decisions about your drug's development. It’s all in the name: Celerion is derived from the Latin celeritas (meaning swiftness and speed), which reflects our founding principle—that fast, reliable research is vital to a product's success.

Celerion’s focus is on the implementation of innovative strategies to generate key data very early to enable go/no-go decisions in drug development. With a large clinical capacity of more than 600 beds, efficient bioanalytical laboratories and experienced scientific staff, Celerion offers one of the most experienced clinical pharmacology research networks in the industry.

Why Join Celerion?

Celerion is one of the most experienced and successful CROs in the world. One of our key assets and greatest resources is the experience and expertise of our employees. Our vision to be the premier provider of early stage drug development solutions will only be achieved by ensuring that we have the brightest minds in the industry working with us.

We are looking for individuals who enjoy working in a fast-paced environment and who demonstrate leadership, teamwork, and are passionate about what they do.

If you want to build a meaningful career in a successfully growing company, and make a positive contribution to the health and well-being of people around the world, join our team.

COMPANY SIZE
1,000 to 1,499 employees
INDUSTRY
Biotechnology/Pharmaceuticals
EMPLOYEE BENEFITS
401K
WEBSITE
https://celerion.com/