Ensure All Study Site Personnel Participating in This Study Are Trained in Good Clinical Practice Requirements and Guidelines for Treatment of Human Subjects, Generally Accepted Professional Standards
STUDY SITE CO-INVESTIGATORS AND RESEARCH STAFF WILL OBTAIN LOCAL IRB APPROVAL FOR THE U01 STUDY; RECRUIT, CONSENT AND ENROLL SUBJECTS IN ACCORDANCE WITH THE PROTOCOL, ICH GCP, AND ALL APPLICABLE STATE
TO PROVIDE QUALITY REUSED ASSISTIVE TECHNOLOGY AND DURABLE MEDICAL EQUIPMENT (DME) TO INDIVIDUALS WITH DISABILITIES. TO MAINTAIN THE LEVEL OF EXPERTISE REQUIRED TO PROVIDE QUALITY EQUIPMENT AND ACCURA
DR. JOHNSTON WILL OVERSEE ALL ASPECTS OF HUMAN SUBJECTS PARTICIPATION. SHE WILL DRAFT THE PROTOCOL, AND ENSURE IRB SUBMISSION, AND WILL RECRUIT, ENROLL, AND RETAIN PARTICIPANTS IN THE CLINICAL STUDY.
"STEPHANIE HOOKER, PHD, MPH (SITE PRINCIPAL INVESTIGATOR) IS A RESEARCH ASSOCIATE AT HEALTHPARTNERS INSTITUTE WITH A BACKGROUND IN CLINICAL HEALTH PSYCHOLOGY AND PUBLIC HEALTH. AS THE SITE PRINCIPAL I
INCORPORATE FAR CLAUSE 52.223-99 AND VHA SUPPLEMENTAL CONTRACT REQUIREMENTS FOR ENSURING ADEQUATE COVID-19 SAFETY PROTOCOLS FOR FEDERAL CONTRACTORS. D1 AMBULANCE TRANSPORTATION SERVICES
EO14042: NEW CLAUSE FOR ENSURING ADEQUATE COVID-19 SAFETY PROTOCOLS FOR FEDERAL CONTRACTORS
Addressing durable health disparities through critical time legal interventions in medically underserved Latinx and migrant communities in the United States.
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40
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Moderate opportunity — established market with selective entry points.