You haven't searched anything yet.
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 support a business creating life-saving treatments? If so, we can't wait to meet you!
Purpose:
As a Quality Control Specialist you are responsible for the review and verification of all source data. Conduct data reconciliation and final check of data. Conducts final quality check and reviews source documentation. Ensures the completeness, accuracy and consistency of source data so that it meets the standards of quality expected for reporting to Sponsors and regulatory bodies. Participate with multidisciplinary teams involved in setting up, conducting and reporting clinical trials. This is a full time position that starts at $19/hour.
\nEssential Functions
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.
Full Time
Scientific Services
$62k-81k (estimate)
05/22/2024
06/01/2024
celerion.com
TEMPE, AZ
500 - 1,000
2010
Private
STEVE HURLEY
$200M - $500M
Scientific Services
Celerion is a Nebraska-based clinical research organization that develops and commercializes drug development and medical writing services for the pharmaceutical sector.