Job Summary
We are seeking a dedicated and detail-oriented Clinical Research Coordinator with experience to join our dynamic research team. In this vital role, you will oversee the planning, coordination, and execution of clinical trials to ensure compliance with regulatory standards and study protocols. Your expertise will facilitate accurate data collection, patient monitoring, and documentation review, contributing to groundbreaking medical advancements. This position offers an exciting opportunity to be at the forefront of clinical development while ensuring participant safety and regulatory adherence.
Duties
- Dispense, administer, maintain pharmacy IP
- Record daily temperatures
- Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits
- Monitor patient progress by recording vital signs, blood sampling, and other clinical assessments in accordance with study protocols
- Review and verify study documentation for accuracy, completeness, and regulatory compliance
- Manage data collection and entry using electronic medical record (EMR) systems and adhere to CDISC standards for data management
- Ensure adherence to FDA regulations, ICH GCP guidelines, and HIPAA privacy rules throughout all trial activities
- Supervise research staff and collaborate with multidisciplinary teams to maintain high-quality trial conduct
- Conduct clinical laboratory procedures such as blood sampling and phlebotomy with precision and safety
Skills
- MUST BE BILINGUAL
- Proven supervising experience in clinical research settings with strong leadership capabilities
- Extensive knowledge of clinical trials management, including regulatory submissions and compliance management
- Proficiency in medical terminology, clinical laboratory techniques, and analysis skills for interpreting data
- Familiarity with statistical software used for data analysis in research environments
- Understanding of FDA regulations, ICH GCP standards, and CDISC data standards for clinical research
- Experience with EMR systems, blood sampling procedures, and patient monitoring techniques
- Strong documentation review skills ensuring accuracy and regulatory compliance in all trial records
Join us to make a meaningful impact on healthcare innovation! We are committed to fostering a vibrant work environment that supports your professional growth while advancing critical medical research. This paid position offers an engaging opportunity to develop your expertise in clinical development while working alongside passionate professionals dedicated to improving lives through science.
Pay: $18.00 - $30.00 per hour
Benefits:
- 401(k)
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Retirement plan
- Vision insurance
Experience:
- Research: 1 year (Required)
Work Location: In person
