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Systimmune
Overview
The Study Startup Specialist coordinates and oversees all aspects of clinical trial initiation, including managing essential document collection, regulatory submissions to bodies like IRB/EC, and tracking startup milestones to ensure sites are ready for patient enrollment on time. This role involves preparing, reviewing, and submitting regulatory documents, supporting contract/budget negotiations, and maintaining audit-ready documentation in systems like eTMF.
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Compensation
$70,000 - $95,000 / YEAR
Posted
9 days ago
QIAGEN
The CRA acts as the primary contact for clinical study sites, managing start-up, monitoring, and high-quality data collection. They ensure research is conducted according to regulatory standards while protecting the rights and safety of human subjects.
$65,000 - $75,000 / YEAR
1 month ago
