The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials
Job Summary
The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials.
Candidates will manage electronic Trial Master Files (eTMF), coordinate Investigator Site File materials, and analyze study metrics to maintain high-quality standards.
This position requires working the third shift (nights) remotely while collaborating with a global team across 100+ countries.
Matching Summary
The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials.
Skills & Requirements
Must-have
eTMF system proficiency
site activation critical path
regulatory compliance knowledge
third shift night work availability
remote work capability
Nice-to-have
strong organizational skills
ability to train new staff
local market knowledge
proactive risk communication
Key Requirements
High school diploma or Bachelor's degree preferred