Sub-I (NP or PA) l Buffalo, NY l Full-Time

Key Responsibilities
Clinical Responsibilities
▪ Interpret clinical protocols
▪ Create telephone screening tools for the call center’s use in pre-screening patients
▪ Create study summaries, providing a basic overview of the research study as a reference
for staff.
▪ Advise on Inclusion/Exclusion set up
▪ Draft correspondence to subjects and follow up letters to primary care physicians
▪ Be familiar with all assigned studies
▪ Be a resource for all staff clinical questions
▪ Review marketing materials and give clinical input
▪ Additional duties and projects as assigned
▪ Conduct study visits with subjects
▪ Adhere to good clinical practices and FDA human subject protection guidelines
▪ Administer Informed Consent
▪ Review and record medical histories
▪ Review and record physical assessments
▪ Review inclusion/exclusion criteria to determine patient eligibility
▪ Review and record medications, indications for use, dates of use
▪ Assess patient compliance with study drug and follow-up visits
▪ Assess patient’s response to therapy
▪ Review and sign off on lab results and tests in consultation with Principal Investigator if
needed
▪ Review ECG’s and provide a provisional interpretation
▪ Assess and document adverse events per company SOPs with final sign off by the Principal
Investigators

▪ Conduct other visit procedures as assigned by supervisor and delegated by Principal
Investigator
▪ May share on-call responsibilities as needed to support subjects in trials
Educational Responsibilities
▪ Train applicable staff on informed consent
▪ Train recruitment/marketing team on telephone screen tools/protocols
▪ Assist in recruitment team training
▪ Assist staff in understanding clinical requirements of the protocol
▪ Attend Investigator’s Meetings for new studies, as needed
▪ Perform “Free Screen” assessments, provide interpretation and education regarding results.
▪ Provide in-services on scientific rationales of studies for clinical staff, as needed.
▪ Develop, attain, and provide patient education regarding the clinical trial process as well as
diseases and treatments
▪ Assist in writing for RCR website and newsletter as needed
▪ Assist with workplace wellness initiatives