Clinical Trials Nursing Specialist

2 weeks ago


Neptune City, New Jersey, United States Hackensack Meridian Health Full time
Position Overview

Clinical Research Nurse

At Hackensack Meridian Health, our dedicated teams strive to enhance the lives of our patients by delivering exceptional care every day. Our extensive range of services enables you to utilize your expertise across various environments while advancing your career within New Jersey's leading healthcare system.

Key Responsibilities
  • Ensure timely submission of all protocol modifications, informed consent documents, ongoing reviews, and serious adverse event reports to the appropriate Institutional Review Board (IRB).
  • Collaborate with regulatory experts and principal investigators on all regulatory matters and protocol modifications.
  • Participate in the assessment of study feasibility alongside the principal investigator, clinical research coordinator, and clinical team, evaluating potential competition with other studies prior to submission.
  • Work with the principal investigator and/or clinical research coordinator to draft a budget that outlines standard care and research expenses, finalizing it with the budget coordinator.
  • Recruit and assess potential study participants, coordinating with the clinical research coordinator to arrange necessary appointments and interviews.
  • Identify and address the specific needs of the patient population served, tailoring care accordingly (considering factors such as age, culture, and sensory impairments).
  • Communicate effectively with patients, caregivers, and primary contacts at their level of understanding (developmental, educational, literacy, etc.).
  • Review medical records for potential study candidates, ensuring documentation of all laboratory results, procedures, and patient progress in compliance with protocol guidelines.
  • Educate potential study participants, caregivers, physicians, and other involved healthcare staff on patient care, available trials, treatments, and associated side effects.
  • Assist the investigator with the consent process, ensuring that study participants comprehend clinical trial details and obtaining written informed consent.
  • Provide education to study participants regarding informed consent procedures and HIPAA authorization.
Qualifications
  • Current and valid New Jersey Nursing license is required.
  • A minimum of 3 years of clinical nursing experience or 1 year of clinical nursing experience coupled with 2 years of clinical research experience is required.
  • Preferred certifications include Certified Clinical Research Professional (CCRP), Certified Clinical Research Associate (CCRA), or Certified Clinical Research Coordinator (CCRC).
  • Education in human subject research and Good Clinical Practice (GCP) is preferred.
  • Familiarity with clinical trials and relevant regulations (local, state, and federal) is preferred.
  • Basic understanding of scientific and healthcare principles and terminology is preferred.
  • A Bachelor of Science in Nursing (BSN) is preferred.

Hackensack Meridian Health is committed to the principles of equal employment opportunity and affirmative action, ensuring non-discrimination in recruitment and employment practices based on race, color, creed, national origin, ancestry, marital status, gender, age, religion, sexual orientation, gender identity/expression, disability, veteran status, and any other category protected by federal or state law.



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