Overview
We are seeking a highly organized and detail-oriented Clinical Research Coordinator to oversee and manage clinical trials within our research facility. The ideal candidate will have a strong background inpatient safety, medical terminology, and compliance with FDA regulations. This role offers an opportunity to contribute to groundbreaking medical research while ensuring adherence to industry standards and protocols. The Clinical Research Coordinator will play a vital role in coordinating study activities, monitoring patient safety, and maintaining accurate documentation to support the integrity of our research projects.
Duties
- Coordinate and oversee all aspects of clinical trials, including patient recruitment, enrollment, and follow-up procedures
- Review and ensure accuracy of study documentation, including consent forms, case report forms, and regulatory documents
- Monitor patient health status, vital signs, blood sampling, and other clinical assessments in accordance with study protocols
- Ensure all activities align with research protocol and objectives
- Maintain accurate and complete source documents, CRFs, and study files.
- Monitor study drug/investigational product accountability.
- Serve as the main point of contact for sponsors, CROs, and regulatory authorities.
- Prepare,pack, and ship patient's samples.
- Prepare for monitoring visits.
- Electronic data entry
Skills
- Experience in a clinical or research setting
- Extensive knowledge of clinical trials management, FDA regulations, ICH GCP standards, and HIPAA compliance
- Proficiency with EMR systems.
- Strong understanding of medical terminology, blood sampling techniques (phlebotomy), vital signs measurement, and clinical laboratory procedures
- Excellent documentation review skills with attention to detail for regulatory submissions and audit readiness
- Experience in patient monitoring including vital signs assessment and adverse event reporting
- Knowledge of clinical development processes.
- Effective communication skills for collaboration across multidisciplinary teams involved in clinical research
- International Medical gradute is a plus
- Bilingual ( spanish) is a plus
This position offers an engaging environment where your expertise will directly impact the advancement of medical science. We seek dedicated professionals committed to maintaining the highest standards of clinical trial conduct. International Medical Gradutes are highly encouraged to apply.
Pay: $20.00 - $26.00 per hour
Benefits:
- 401(k)
- Health insurance
- Paid time off
Education:
Language:
Work Location: In person
