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:

Master's (Preferred)

Ability to Commute:

Daytona Beach, FL 32117 (Preferred)

Ability to Relocate:

Daytona Beach, FL 32117: Relocate before starting work (Preferred)

Work Location: In person

Arrow Clinical Trials

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Psychometric Rater/ Clinical Research Coordinator