Clinical Research Coordinator
On-site · Corpus Christi, Texas, United States
Corpus Christi, Texas, United StatesOn-siteFull TimeMid LevelHigh School Or EquivalentUnknown
Type
Full Time
Level
Mid Level
Education
High School Or Equivalent
Company size
Unknown
Job Summary
Coordinate and manage the day-to-day operations of assigned clinical trials, recruit and screen participants, ensure compliance with study protocols and regulatory requirements (FDA, ICH GCP, HIPAA), document and report on study activities, track enrollment, and liaise with pharmaceutical sponsors and external vendors. Requires strong communication, organizational skills, and a collaborative, proactive approach; reports to the Clinical Operations Manager.
Required Qualifications
- High school diploma or GED
- 1 year of experience as a Clinical Research Assistant or Coordinator
- 1-2 years of experience in Clinical Research
- Proficient in Microsoft Office applications and CRIO or equivalent CTMS
- Must have strong knowledge of ICH/GCP guidelines
- Must complete GCP training before interacting with participants and recertify every 2 years or as applicable
- Trained and certified in Fibroscan and memory screens as required by the study portfolio and individual experience; training to be provided
- Must have basic life support (BLS) training, provided during onboarding
- Demonstrated organizational skills and time management with ability to track multiple projects
- Strong written and oral communication skills
- Knowledge of basic medical terminology
- Valid Driver’s License
- Bilingual in Spanish and English preferred
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