Research Specialist II - FT - Days - MCI

Memorial Healthcare • Pembroke Pines, FL

2d • Onsite

About The Position

Conducts Phase 1-4 Clinical Trials for patients and captures study-related data for sponsors. The role involves obtaining medical history, monitoring patient care, assessing ongoing patient status, and monitoring treatment side effects. The specialist documents patient/study results using the electronic medical record (EPIC) and completes data requirements for sponsors, while also communicating patient/study results on an ongoing basis to the research team. This position coordinates activities of a multidisciplinary team that cares for the patient, as well as patient visits and necessary testing. The role includes conducting initiation, monitoring, and close-out visits with sponsors, collaborating to ensure compliance with local, state, and federal regulations and standards, and assisting with preparing for and responding to audits. The specialist participates in audits, reports adverse events, and resolves data queries with sponsors. Additionally, they process and ship study-required specimens, screen and consent patients for clinical trials using Good Clinical Practice (GCP) guidelines, and provide patient and family support and education regarding protocol-related drugs and procedures.

Requirements

• Accredited Program (Required)
• Foreign Medical Doctor Degree (FOREIGN MD DEGREE) - Classroom Training (CLASSROOM TRAINING)
• Registered Nurse License (RN LICENSE) - State of Florida (FL)
• 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.
• Must be able to work in a stressful environment and take appropriate action.
• One (1) year of clinical experience.
• At least two (2) years of clinical research experience.
• 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

Responsibilities

• Obtains medical history, monitors patient care, assess ongoing patient status and monitors treatment side effects.
• 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.
• Coordinate 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 patient's for clinical trials using Good Clinical Practice (GCP) guidelines. Provides patient and family support and education regarding protocol related drugs and procedures.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree