Research Specialist II - FT - Days - MCI

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

Responsibilities

Obtains medical history; Monitors patient care; Assesses ongoing patient status; Monitors treatment side effects; Documents patient/study results using electronic medical record (EPIC); Completes data requirements for sponsors; Communicates patient/study results on an ongoing basis to research team; Coordinates activities of multidisciplinary team that cares for the patient as well as patient visits and necessary testing; 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; 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

Requirements

Accredited Program; Foreign Medical Doctor Degree (Classroom Training); Registered Nurse License - State of Florida (FL); One (1) year of clinical experience; At least two (2) years of clinical research experience; Ability to travel for protocol related investigator meetings and research related training; Critical thinking skills; Effective communication; Decisive judgement; Ability to work with minimal supervision; Ability to work in a stressful environment and take appropriate action; Proof of Graduation certificate for foreign trained MDs or equivalents clinical programs; Graduate from an accredited professional nursing program or Foreign Medical doctor program or Equivalent relevant degree