CTMS Entry Coordinator
On-siteFort Worth, Texas, United States
Job Summary
Collect, de-identify, and enter clinical data into electronic case report forms, including images, lab results, and ECGs, while resolving queries. Collaborate with Clinical Research Coordinators to ensure accurate data timepoints and contact patients for follow-up as needed. Review protocols to guide study activities, assist with formatting eligibility documents and study schedules, and maintain CTMS records for patient visits, IRB re-consents, and adverse events. Provide support to onsite and remote monitors, communicate with accounts receivable regarding transmitted data, and attend site initiation visits and roster meetings. Comply with all regulations pertaining to data loading and EDC systems.
Required Qualifications
- High School diploma or equivalent
- One year of research administrative experience within a healthcare, pharmaceutical, or research organization
- Knowledge and training in general office administration skills, including computer applications, filing systems, etc.
- Familiarity with medical terminology
- Strong organizational skills and a sense of timeliness in completing projects
- Detail-oriented
- Ability to understand instructions
- Ability to work independently
- Must be able to lift 50 lbs
Desired Qualifications
- Bachelor's degree
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