Title: Nurse Practitioner โ Remote Research Study Reviewer
Position: Remote - Part Time
Work Hours:
- Anticipate up to 10 participants per week
- Each participant review is anticipated to require approximately 30 minutes to 1 hour
- Flexible remote schedule, in coordination with research staff and participant schedules
Pay range: $40.00/hr. - $44.44 /hr.
Job Description:
Position Summary:
The individual will remotely review participant eligibility, assess inclusion and exclusion criteria, and assist with protocol-directed clinical oversight for research participants.
This position is ideal for a clinician with experience in clinical research, protocol compliance, and telemedicine-based participant interactions.
Primary Responsibilities:
- Review participant medical information to determine eligibility based on study inclusion and exclusion criteria.
- Conduct remote/telemedicine-based participant assessments as required by study protocols.
- Review and authorize serial blood draws according to protocol requirements.
- Coordinate or assist with ordering medical and research-related supplies.
- Document eligibility determinations and protocol reviews in accordance with institutional and regulatory requirements.
- Communicate with study coordinators and research staff regarding participant eligibility and protocol compliance.
- Ensure adherence to human subjectโs research regulations and institutional policies.
Required Qualifications:
- Current licensure as a Nurse Practitioner in New York.
- Strong clinical judgment and attention to detail.
- Ability to work independently in a remote environment.
- Excellent written and verbal communication skills.
Required Training
- Current CITI Human Subjects Research Training certification required prior to study participation.
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Preferred Qualifications
- Experience with telemedicine platforms.
- Experience working on academic or federally funded research studies.
- Experience with clinical research and/or human subjectโs research.
- Experience reviewing laboratory and medical history data for study eligibility.
- Experience with IRB-regulated clinical research environments.
- Experience or familiarity with research protocols and inclusion/exclusion review processes.