The Clinical Research Coordinator will coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for Huntington’s Disease research
Job Summary
The Clinical Research Coordinator will coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for Huntington’s Disease research.
This position will draft and maintain IRB submissions, including initial applications, amendments, and continuing reviews, and manage informed consent language and documentation across multiple protocols.
The role involves organizing, curating, and quality controlling longitudinal neuroimaging datasets for Huntington’s Disease cohorts and preparing and curating datasets for statistical and machine learning analyses.
Matching Summary
The Clinical Research Coordinator will coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for Huntington’s Disease research.
Skills & Requirements
Must-have
Coordinate clinical research activities
Recruit and enroll patients
Obtain informed consent
Collect and process biological samples
Administer diagnostic testing
Monitor adverse reactions
Maintain IRB submissions
Nice-to-have
Interest in data management
Experience with scripting
Familiarity with version control
Interest in machine learning applications
Key Requirements
Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience
1 year of relevant experience
Clinical research certification from an accredited certifying agency desired (ACRP or SOCRA)