Nurses with experience in any of the following areas are strongly encouraged to apply: Clinical trial or study, Oncology, or Peer review.
Shift(s) available: day shift, night shift, and mid shift
Job types available: full time, part time, and per diem
Responsibilities:
Coordinate and manage patient care in line with protocol requirements, working closely with Principal Investigators and other healthcare professionals
Screen potential study participants and obtain informed consent prior to enrollment in research studies Administer study treatments, collect biological samples, and monitor participants throughout the study
Maintain accurate and timely documentation, including case report forms, medication logs, and adverse event report
Collaborate with the research team to ensure compliance with ethical standards and regulations, and to prepare for audits and inspections
Qualifications:
Bachelor's Degree in Nursing (BSN) or higher
Active and unencumbered Registered Nurse license
2+ years of clinical nursing experience preferred
Prior experience in a clinical research setting preferred
Strong communication skills, both written and verbal, to effectively convey information to study participants, research staff, and stakeholders
| Location | New Jersey |
| Website | https://www.skyelia.com |
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