Clinical Research Assistant Jobs in San Antonio, TX

Job Summary

We are seeking a dynamic and detail-oriented Clinical Research Coordinator to join our innovative research team. In this vital role, you will oversee the planning, execution, and management of clinical trials, ensuring adherence to regulatory standards and ethical guidelines. Your proactive approach will facilitate seamless communication among stakeholders, coordinate study activities, and maintain meticulous documentation. This position offers an exciting opportunity to contribute to groundbreaking healthcare research that impacts patient outcomes worldwide. The ideal candidate is energetic, highly organized, and passionate about advancing clinical science through rigorous research practices.

Duties

• Coordinate all aspects of clinical trials, including participant recruitment, enrollment, and follow-up procedures in compliance with FDA regulations and ICH GCP standards
• Supervise research staff and oversee training to ensure adherence to clinical research methods and ethical guidelines
• Review and verify clinical documentation, including informed consent forms, case report forms, and regulatory documents for accuracy and completeness
• Monitor patient progress throughout the study duration, including blood sampling, data collection, and adverse event reporting
• Manage data entry, validation, and analysis using statistical software while ensuring compliance with CDISC standards and data management protocols
• Maintain accurate records within electronic medical record (EMR) systems and ensure HIPAA compliance for patient confidentiality
• Conduct regular quality assurance checks to uphold clinical trial standards and ensure compliance with healthcare regulations

Skills

• Supervising experience in a clinical or research setting with proven leadership capabilities
• Strong knowledge of medical terminology and clinical laboratory procedures
• Expertise in reviewing clinical documentation and conducting patient monitoring activities
• Proficiency with statistical software for data analysis and interpretation
• Familiarity with FDA regulations, ICH GCP guidelines, and healthcare compliance standards such as HIPAA
• Experience with clinical development processes, project management in healthcare environments, and research project coordination
• Ability to utilize Microsoft Office suite effectively for reporting and documentation purposes
• Certification in ICH GCP (from a recognized issuer) or equivalent certification such as CA (California) certification is highly desirable
• Knowledge of EMR systems, blood sampling techniques, CDISC standards for data collection, and clinical trials management systems
• Strong understanding of clinical ethical guidelines, compliance management practices, and quality assurance standards in research settings
• Excellent analysis skills combined with attention to detail to ensure data integrity and research accuracy

Join us in advancing health sciences by coordinating impactful clinical trials that make a difference! We are committed to fostering a collaborative environment where your expertise drives innovation while supporting your professional growth. This paid position offers an engaging opportunity to be at the forefront of clinical research excellence.

Pay: $20.00 - $25.00 per hour

Benefits:

• Flexible schedule
• Professional development assistance

Experience:

• Clinical Research Coord.: 1 year (Required)

License/Certification:

• GCP Certification (Required)

Location:

• San Antonio, TX 78229 (Required)

Work Location: In person