Dynamic duo enhances ARAC’s capabilities, offering facility trainings and on-site clinical assessments (i.e., urine analysis and other biomarkers of exposure). This new team is yet another demonstration of ARAC’s commitment to ensure a successful project implementation and ethical conduct focused on human subject protections.
KEY RESPONSIBILITIES include:
Remote monitoring of Adverse Events and clinical assessments of side effect severity related to research study product use
Oversee compliance to IRB-approved study protocols
Lead research site trainings at study facilities
Quality assurance to ensure ethical conduct
LEARN MORE > https://lnkd.in/e_TMZXHQ
SCHEDULE A MEETING > https://calendly.com/arac4
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