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Clinical Research Coordinator

2 months ago

Brooklyn, New York, United States DM Clinical Research Full time
Job Overview

The Sub-Investigator (Nurse Practitioner) is a key member of the DM Clinical Research team, responsible for ensuring adherence to protocol requirements and protecting the rights and welfare of subjects.

Key Responsibilities
  • Completing required training, including GCP and IATA, to maintain a working knowledge of current FDA regulations, GCP/ICH guidelines, and organizational SOPs.
  • Maintaining a current, up-to-date curriculum vitae and current licensure to practice.
  • Assisting in managing the activities and performance of clinical staff affiliated with the site.
  • Performing clinical-related procedures and/or making important trial-related decisions delegated by the Principal Investigator.
  • Performing clinical safety assessments and monitoring for study trial participation, including physical exams, EKGs, phlebotomy, and lab work evaluation.
  • Possessing a thorough understanding of the requirements of each protocol.
  • Managing the medical care of subjects and protecting their rights and welfare.
  • Ensuring documentation of study-related procedures, processes, and events.
  • Attending investigator meetings as necessary for study participation.
Requirements
  • Bachelor's or Master's degree in Nursing.
  • Previous clinical research experience.
  • Nursing experience in a clinical setting.
  • Current nursing licensure in good standing (Nurse Practitioner).
Preferred Qualifications
  • Basic clinical and patient care skills.
  • Knowledge of nursing and medical principles and techniques.
  • Clinical research knowledge.
  • Strong communication skills, both written and verbal.
  • Strong diagnostic skills.
  • Ethical and legal healthcare principles in patient care.