Human Sub Research Spec II

The NMD Study Coordinator II will manage projects in peripheral neuropathies, CMT and ALS. The research projects in the group include observational studies, clinical trials, and multi-center clinical research studies. The Study Coordinator II will have considerable latitude for independent judgment and coordinates all aspects of assigned human subject research studies. This role provides assistance to the Principal Investigator(s) and works as an integral part of the research team. This role mentors Human Subject Research Coordinator I(s) and supervises students as assigned.

Responsibilities

Manage projects in peripheral neuropathies, CMT and ALS; Recruit, consent, enroll and retain study subjects across the NMD portfolio; Coordinate, schedule and conduct research study visits according to the protocol; Mentor and train NMD Study Coordinators (HSRC I); Develop, modify and maintain regulatory requirements for multiple research studies; Manage IRB submissions including applications, amendments and continuing reviews; Serve as liaison between research team, research sites, research administration, study sponsors and IRB; Develop and/or manage databases for research studies; Demonstrate accountability for continuous learning related to clinical research; Other duties as assigned

Requirements

Bachelor's degree and 2 years of experience in human subject research coordination; Or equivalent combination of education and experience; If applicable, department specific experience; Word processing and data analysis software

Nice to have

Experience as Human Subject Research Coordinator I; Experience as a Phlebotomist; SOCRA Certification in Clinical Research (upon hire); Association of Clinical Research Professionals (ACRP) certification (upon hire)