Essential Functions
- Attend study setup meetings to determine QC criteria and timelines for each study
- Review study-specific source documents to ensure all forms are accurate prior to study start and that all data collected is in accordance with study-specific Case Report Forms and protocol requirements.
- Ensure QC reviews are complete in accordance with study-specific timelines
- Review source data on an ongoing basis to ensure the following: Clinical source data is complete according to GCP and FDA guidelines, protocol deviations (if applicable) are documented, and source data is collected in accordance with Sponsor requirements, and Celerion SOPs/PGs. Ensure data corrections are completed according to GCP guidelines, and Celerion SOPs/PGs. Complete a Final QC to ensure all source data is accounted for and has been QC reviewed
- Perform accurate data entry and verification for Celerion Standard and Sponsor Provided EDCs.
- Archive source documentation including CRFs
- Complete QC/DE dedicated milestones in a timely manner
- Perform standard quality control steps
Requirements
- High School Diploma or GED (relevant internal Celerion experience in lieu preferred)
- 1 - 2 years industry experience preferred
- Previous Quality Control/ Data Entry or related experience preferred
- Medical Terminology Training preferred
- Excellent oral and written communication skills
- Ability to organize and manage multiple priorities
- Experience working in an environment with complex processes and defined criteria
- Excellent time management skills required
- Proficient in MS Office applications required
- Excellent attention to detail skills required
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