Clinical Research Provider
2 months ago
The Clinical Research Provider (CRP) works collaboratively with members of the CND team to help conduct three areas of scientific research for the company: (a) IRB-approved clinical studies (b) IRB-approved exploratory research programs involving human subjects and (c) quality improvement initiatives involving healthy human subjects. The Clinical Research Provider plays a lead role in the assessment, treatment, and evaluation of human subjects enrolled in these approved research areas, including but not limited to the collection of punch skin biopsies consistent with the company's validated diagnostic test protocols. The CRP applies years of clinical training and well-honed research practices and procedures in interaction with patient-subjects and healthy individuals participating in approved research areas and maintains high standards of professionalism as a licensed clinician at all times.
Job Responsibilities:
- Participates in different parts of research programs, studies and initiatives including but not limited to subject recruitment, eligibility verification and enrollment of individual subjects, clinical assessment, management of subjects' symptoms due to adverse events and basic treatment as defined in approved protocols.
- Plays a primary role in the collection of small skin biopsy samples from patient-subjects according to approved protocols, performed at approved and authorized clinical office facilities.
- Interprets approved protocols and the Investigator Brochure.
- Records required data on subjects, as defined by specific research protocols, through eDC and other data collection vehicles.
- Ensures quality and subject safety through ethical conduct.
- Complies will all medical duties as per protocol including CND's SOPs, OSHA, GCP and local regulations.
- Ensures potential study risks are escalated to the Clinical Program Manager (CPM).
- Other duties as assigned.
Knowledge, Skills & Experience:
- A minimum of 5 years of clinical research experience as an Investigator or Sub-Investigator within a health system, life sciences company or CRO
- Therapeutic experience in neurology with expertise in movement disorders are strongly preferred.
- Eligible to see patients and performance procedures in the US
- Experience in Phase I, II or III clinical studies for drug development or large-scale validation studies required.
- Significant experience and comfort in conducting skin biopsy procedures.
- Experience with NIH and other government sponsored protocols a plus
- Strong patient communication skills.
- CITI GCP certification or willing to complete within first month or hire.
Education, Certifications & Licensures:
- Current unrestricted license to practice as a NP, PA, MD or DO in Arizona.
- Bachelor of science degree in relevant field.
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