Remote Nephrology Np Jobs in Rochester, NY (NOW HIRING)

Title: Nurse Practitioner – 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 subject’s 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.

Preferred Qualifications

• Experience with telemedicine platforms.
• Experience working on academic or federally funded research studies.
• Experience with clinical research and/or human subject’s 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.

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