Clinical Research/Clinical Trial () RN

Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”

During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.

Complete study medication order forms accurately, when needed, and has physician or appropriate designee sign orders prior to medication administration

Perform routine operational activities for multiple research protocols

Liaise between site research personnel, industry sponsors, and Supervisor

Collaborate closely with various site departments / teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable

Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout

Coordinate submission and approval for the Site’s Facility Review Committee, if applicable

Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data to physicians, nurses, and clinical staff

Assess the patient and document findings at each clinic visit while on protocol

Document all specific tasks required by the protocol (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.)

Complete the study medication order form accurately and have the physician or nurse practitioner sign orders prior to treatment

Ensure that all medications are approved by the appropriate designee prior to initiating treatment or when changing medication regimens

Accurately calculate and document the BSA, creatinine, STS calculation, or any other conversions needed, per protocol

Document any interaction regarding the patient that occurs while the patient is enrolled on a protocol, including follow-up and survival (this includes home health intervention, pharmacies, and patient phone calls)

Ensure that follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements

Accurately complete all data requests (including queries) and submit with source documentation within the timeframe specified in the SOP

Generate and track drug shipments, device shipments, and supplies as needed

Ensure timely and accurate data completion

Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations

Communicate all protocol-related issues to appropriate study personnel or manager

Re-consent patients in a timely manner and document process appropriately

Salary : $1,574