Research Associate

2 months ago


Jersey City, New Jersey, United States DM Clinical Research Full time
Job Summary

We are seeking a highly skilled and experienced Sub-Investigator (Nurse Practitioner) to join our team at DM Clinical Research. As a key member of our clinical research team, you will be responsible for ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, and directing the conduct of research according to federal and state regulations and guidance documents.

Key Responsibilities
  • Protocol Management: Ensure adherence to protocol requirements, including completing DMCR-required training, maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols.
  • Subject Care: Manage the medical care of subjects, protect their rights and welfare, and ensure documentation of study-related procedures, processes, and events.
  • Team Leadership: Assist in managing the activities and performance of the clinical staff affiliated with the site, and attend investigator meetings as necessary for study participation.
  • Clinical Research Knowledge: Possess a thorough understanding of the requirements of each protocol, and maintain a current, up-to-date curriculum vitae and current licensure to practice.
Requirements
  • Education: Bachelor's or Master's degree in Nursing.
  • Experience: Previous clinical research experience and nursing experience in a clinical setting.
  • Credentials: Current nursing licensure in good standing (Nurse practitioner).
  • Knowledge and Skills: 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, and ethical and legal healthcare principles in patient care.


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