Job Summary
We are seeking an experienced, dedicated and detail-oriented Clinical Research Coordinator and Psychometric Reader to join our team. The ideal candidate will play a crucial role in managing clinical trials while performing specialized subject ratings to ensure accurate data collection and high-quality trial conduct. This position requires strong organizational skills, a solid understanding of clinical research processes, rating assessments and the ability to effectively work well with team members while maintaining high standards of patient care.
Duties
- Coordinate day-to-day clinical trial operations, including scheduling visits, maintaining regulatory compliance, and ensuring protocol adherence.
- Ensure compliance with FDA regulations, Good Clinical Practice (GCP), and HIPAA guidelines throughout the research process.
- Conduct patient assessments including vital signs, phlebotomy, and blood sampling as necessary.
- Review and manage clinical documentation to ensure accuracy.
- Utilize statistical software for data analysis and management of research findings.
- Collaborate with cross-functional teams to facilitate effective communication and coordination within the clinical development process.
- Maintain electronic medical records (EMR) systems to ensure accurate tracking of patient information and trial progress.
- Monitor patient safety throughout the study by conducting regular follow-ups and assessments.
- Perform rater assessments across neurological, psychiatric, and pain-related studies, following protocol-specific scales and procedures.
- Collect, document, and maintain accurate subject data in accordance with GCP, FDA, and sponsor guidelines.
- Collaborate with investigators, sponsors, and CROs to ensure smooth study execution and timely deliverables.
- Provide study participants with professional support, ensuring safety and a positive experience throughout trial participation.
- Support startup, monitoring, and close-out visits, including regulatory documentation and site readiness.
Experience
Candidates should possess a strong background in clinical research with experience in the following areas:
- Clinical trials management including knowledge of regulatory requirements.
- Familiarity with medical terminology and clinical laboratory practices.
- Proficiency in data management techniques and documentation review processes.
- Experience with patient monitoring techniques and compliance management.
- Demonstrated ability to administer standardized rating scales with reliability.
Job Types: Full-time, Part-time
Pay: $24.35 - $35.00 per hour
Expected hours: 40 per week
Benefits:
- 401(k)
- Health insurance
- Paid time off
Education:
Ability to Commute:
- Daytona Beach, FL 32117 (Preferred)
Ability to Relocate:
- Daytona Beach, FL 32117: Relocate before starting work (Preferred)
Work Location: In person