Job Description

Summary:

Conducts Phase 1-4 Clinical Trials for patients and captures study-related data for sponsors.

Responsibilities:

• Conducts initiation, monitoring and close out visits with sponsors. Collaborates to ensure compliance with local, state and federal regulations and standards. Assists with preparing for and responding to audits. Participates in audits. Reports adverse events and resolves data queries with sponsors. Processes and ships study required specimens.
• Coordinates activities of multidisciplinary team that cares for the patient as well as patient visits and necessary testing.
• Documents patient/study results using the electronic medical record (EPIC) and completes data requirements for sponsors. Communicates patient/study results on an on-going basis to research team.
• Screens and consents patients for clinical trials using Good Clinical Practice (GCP) guidelines. Provides patient and family support and education regarding protocol related drugs and procedures.
• Obtains medical history, monitors patient care, assesses ongoing patient status and monitors treatment side effects.

Education and Certification Requirements: Accredited Program (Required)Foreign Medical Doctor Degree (FOREIGN MD DEGREE) - Classroom Training (CLASSROOM TRAINING), Registered Nurse Compact License (RN LICENSE COMPACT) - Compact RN Multistate, Registered Nurse License (RN LICENSE) - State of Florida (FL)

Required Work Experience: One (1) year of clinical experience. At least two (2) years of clinical research experience. Other Information: **Proof of Graduation certificate for foreign trained MDs or equivalents clinical programs.

Additional Education Info: Graduate from an accredited professional nursing program or Foreign Medical doctor program or Equivalent relevant degree

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