Clinical Research Coordinator

Job Summary
We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and maintaining the highest quality of data collection. Your expertise will help advance innovative medical treatments and improve patient outcomes through meticulous coordination and collaboration with multidisciplinary teams. This position offers an exciting opportunity to contribute to groundbreaking research in a fast-paced, supportive environment dedicated to excellence in clinical development.

Duties

• Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits
• Ensure adherence to FDA regulations, ICH GCP guidelines, and institutional policies throughout the trial process
• Review and verify study documentation, including consent forms, case report forms, and regulatory submissions
• Monitor patient safety by tracking vital signs, blood sampling (phlebotomy), and adverse event reporting
• Manage data collection and entry using EMR (Electronic Medical Records) systems and ensure data accuracy in compliance with CDISC standards
• Supervise research staff and collaborate with investigators to facilitate smooth trial operations
• Conduct clinical laboratory procedures and analyze laboratory results to support study objectives
• Maintain detailed records of trial activities, monitor protocol compliance, and prepare reports for regulatory audits
• Oversee patient monitoring activities to ensure participant well-being and protocol adherence
• Utilize statistical software for data analysis and contribute to research publications or presentations

Requirements

• Bachelor’s degree in Nursing, Life Sciences, or related field; advanced degrees preferred
• Proven supervising experience in clinical research or healthcare settings
• Strong knowledge of clinical trials management, FDA regulations, GCP, and HIPAA compliance
• Experience with clinical laboratory procedures, blood sampling (phlebotomy), and vital signs measurement
• Familiarity with EMR systems, data management tools, and statistical analysis software
• Certification in ICH GCP (Good Clinical Practice) from a recognized issuer; valid CA GCP certification is a plus
• Excellent understanding of medical terminology and documentation review processes
• Ability to coordinate multiple tasks efficiently while maintaining attention to detail
• Strong communication skills for effective collaboration with research teams, participants, and regulatory bodies

Join us in advancing healthcare through innovative research! We are committed to fostering an inclusive environment where your skills can thrive. This paid position offers comprehensive training opportunities and the chance to make a meaningful impact on patient care worldwide.

Pay: $25.00 - $30.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible schedule
• Health insurance
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance

Work Location: In person