Nurse Practitioner for Clinical Studies

2 weeks ago


Ridgewood, New Jersey, United States Medix™ Full time

Medix™ is looking for a dedicated Nurse Practitioner or Physician Assistant to join our team as a Sub Investigator at a leading clinical research facility focused on cognitive trials.

Key Responsibilities:

  • Collaborate with affiliated research institutions.
  • Ensure confidentiality of subjects and documentation, adhering to sponsor requirements and regulatory standards including FDA regulations, good clinical practices, ICH guidelines, HIPAA, and institutional policies.
  • Conduct study-related tasks such as physical assessments, obtaining informed consent, gathering subject history, monitoring adverse events, managing test articles, scheduling appointments, reviewing records, coordinating treatments, collecting vital signs, and performing health evaluations.
  • Maintain comprehensive knowledge of study protocols and related activities.
  • Follow study protocols and regulatory guidelines consistently.
  • Assist in preparing for monitoring visits by study sponsors.
  • Engage in subject screening and recruitment processes.
  • Exercise professional judgment within the parameters set by clinical trial protocols and under the guidance of the principal investigator.
  • Interact with a variety of stakeholders including physicians, nursing staff, administrative personnel, industry sponsors, laboratory and imaging teams, and clinical trial participants.
  • Manage multiple projects with competing priorities and deadlines as dictated by clinical trial protocols and study requirements.

Qualifications:

  • Possession of a valid NJ Nurse Practitioner or Physician Assistant license.


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