Clinical Research Coordinator II
On-site · Pasadena, Texas, United States
Job Summary
Clinical Research Coordinator II leads the site-level clinical research program, recruiting and enrolling research patients under the clinical direction of the principal investigator, ensuring compliance with SOPs, protocol specifications, and GCP. Develops workflows to optimize recruitment and study execution, prescreens patients, trains staff, collaborates with central enrollment, maintains documentation (CRFs, data entry) according to ALCOA, and handles adverse/serious adverse event reporting to IRB/Sponsor. Requires knowledge of medical terminology, GCP, IATA and FDA regulations; ability to perform basic procedures (blood work, vitals, ECG) and collect specimens; strong organizational and communication skills; CKD/nephrology experience is a plus; on-site in Pasadena, TX. Falls under on-site, full-time Clinical role with emphasis on enrollment targets, data integrity, and cross-functional coordination.
Required Qualifications
- MA Certification preferred
- Bachelor’s degree in health-related field preferred
- Good Clinical Practice and or ITIA Certification preferred
- ACRP or Socra Certification preferred
- Bilingual preferred (Spanish)
- Minimum 3 year’s to 5 year’s clinical research experience
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