Clinical Research Associate- San Antonio / South-Central Texas Region Job at Bristol Myers Squibb, Houston, TX

  • Bristol Myers Squibb
  • Houston, TX

Job Description

Bristol Myers Squibb seeks a Clinical Research Associate to oversee clinical trial site quality, integrity, and regulatory compliance across the San Antonio and South-Central Texas region. The role involves site monitoring, data verification, regulatory adherence, and stakeholder management to ensure adherence to protocols and GCP guidelines.

Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits across trial phases
  • Verify data accuracy and completeness in electronic and paper records to ensure protocol compliance
  • Monitor site adherence to ICH GCP, local regulations, and ALCOA principles; provide training as needed
  • Build relationships with internal teams and external partners; represent organization at site level
  • Assess investigator capabilities, identify new sites, and support risk-based monitoring strategies

Requirements

  • Bachelor's degree, preferably in life sciences or equivalent
  • 2-3 years of clinical research experience working independently
  • Valid driver's license as required locally
  • Knowledge of ICH/GCP guidelines and applicable clinical trial regulations
  • Proficiency with data analysis and technology platforms
  • Experience with clinical study coordination or pharma/biotech sponsor roles preferred
  • AI experience or foundational knowledge strongly preferred

Job Tags

Local area

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