Celerion
Clinical Data Specialist
Tempe, AZ
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odds of building a lasting career here
Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
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About the role
- 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.
- Responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF).
Skills
- Attend study setup meetings to determine QC criteria and timelines for each study
- Ensure QC reviews are complete in accordance with study-specific timelines
- Archive source documentation including CRFs
- Complete QC/DE dedicated milestones in a timely manner
- Perform standard quality control steps
Visa & Work Authorization
- and FDA guidelines, protocol deviations (if applicable) are documented, and source data is collected in accordance with Sponsor requirements, and Celerion SOPs/PGs
This listing is sourced directly from Celerion's careers page and normalized into a canonical job model.