Job Summary
We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the coordination and management of clinical trials, ensuring compliance with regulatory standards and maintaining high-quality data collection. Your expertise will facilitate the successful execution of research studies, contributing to advancements in medical science and patient care. The ideal candidate is proactive, organized, and passionate about advancing clinical research initiatives.
Duties
- Coordinate all aspects of clinical trials, including participant recruitment, scheduling, and follow-up visits to ensure smooth study operations
- Review and verify clinical documentation for accuracy, completeness, and regulatory compliance, including informed consent forms and case report forms
- Monitor patient progress by tracking vital signs, blood sampling, and other clinical assessments while ensuring adherence to study protocols
- Manage data collection and entry using electronic medical record (EMR) systems and adhere to CDISC standards for data consistency and quality
- Conduct patient monitoring activities, including phlebotomy procedures and blood sampling, while maintaining strict compliance with HIPAA regulations to protect patient privacy
- Supervise research staff and coordinate with multidisciplinary teams to ensure adherence to FDA regulations, ICH GCP guidelines, and institutional policies
- Utilize statistical software for data analysis, prepare reports for regulatory submissions, and support clinical development efforts through meticulous documentation review
Qualifications
- Proven supervising experience in a clinical research setting or healthcare environment
- Strong knowledge of clinical trials management, including FDA regulations, ICH GCP standards, and HIPAA compliance
- Familiarity with medical terminology, clinical laboratory procedures, blood sampling techniques (phlebotomy), and vital signs measurement
- Experience with EMR systems, data management tools, and statistical software used in clinical research
- Certification in ICH GCP (Good Clinical Practice) from a recognized issuer or equivalent certification valid for California is required
- Background in nursing or related healthcare field preferred; clinical laboratory experience is a plus
- Excellent analysis skills with attention to detail for accurate data collection and review
- Ability to supervise staff effectively while fostering a collaborative team environment
Join us in advancing groundbreaking medical research! This paid position offers an exciting opportunity to contribute meaningfully to clinical development projects that impact patient outcomes worldwide. We value energetic professionals eager to make a difference through meticulous coordination, compliance management, and innovative research support.
Job Type: Full-time
Pay: $22.00 - $25.00 per hour
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Application Question(s):
- Do you hold a current phlebotomy license or certification? Please include the issuing authority and expiration date.
Experience:
- Clinical research coordinator: 2 years (Required)
License/Certification:
- GCP (Good Clinical Practice) certificate (Required)
Ability to Commute:
- Huntington Park, CA 90255 (Required)
Work Location: In person
