Phlebotomist / Clinical Research Coordinator (CRC)

Phlebotomist / Clinical Research Coordinator (CRC)
Location: 2552 Walnut Ave ,Tustin, CA 92780(On-site)
Job Type: Full-Time
Pay: $19-$22/hr (based on experience)

Overview
Join our dynamic healthcare team as a Phlebotomist / Clinical Research Coordinator (CRC), where you'll play a vital role in advancing clinical research and providing exceptional patient care. This position offers an exciting opportunity to combine hands-on blood sampling with coordinating clinical trials, ensuring compliance with regulatory standards and maintaining high-quality data collection. You'll be at the forefront of innovative medical research, supporting the development of new therapies and treatments while fostering a patient-centered environment. This paid position is ideal for motivated individuals eager to make a meaningful impact in clinical development and research.

Duties

• Perform blood sampling and phlebotomy procedures with precision, adhering to established protocols and safety standards
• Coordinate and manage clinical trial activities, including patient recruitment, scheduling, and follow-up assessments
• Monitor patient vital signs and overall health status during study visits, documenting findings accurately in electronic medical records (EMR) systems
• Review and verify clinical documentation for completeness, accuracy, and regulatory compliance, including consent forms and case report forms
• Ensure adherence to FDA regulations, ICH Good Clinical Practice (GCP), and HIPAA privacy standards throughout all trial activities
• Supervise junior staff or team members involved in data collection, specimen handling, or patient monitoring tasks
• Utilize statistical software and CDISC (Clinical Data Interchange Standards Consortium) standards for data management and analysis support

Qualifications

• Proven experience in phlebotomy, blood sampling, or clinical laboratory procedures with strong analysis skills
• Prior experience managing or coordinating clinical trials or research projects in a healthcare setting
• Knowledge of medical terminology, clinical development processes, and regulatory requirements such as FDA regulations and ICH GCP certification
• Familiarity with EMR systems, data collection tools, and compliance management practices including HIPAA guidelines
• Supervising experience or demonstrated leadership skills in clinical or research environments preferred
• Certification in GCP from a recognized issuer (e.g., ACRP or SOCRA) is highly desirable
• Strong organizational skills with attention to detail for documentation review and data management tasks
• Ability to communicate effectively with patients, team members, and regulatory bodies while maintaining confidentiality

Embark on a rewarding career where your expertise directly contributes to groundbreaking medical advancements. We are committed to supporting your professional growth through comprehensive training and fostering an inclusive environment dedicated to excellence in clinical research.

Pay: $19.00 - $22.00 per hour

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Work Location: In person