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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
Hospital for Special Surgery
The Research Assistant will support clinical research activities by managing data collection, facilitating regulatory compliance, and assisting with patient care coordination. They will also act as a clinician's scribe in the operating room to capture vital intraoperative data.
$23 - $36 / HOUR
1 month ago
Medpace, Inc.
The Administrative Assistant will provide day-to-day support with general contract administrative duties and assist with the preparation of final contract documentation. They will also conduct quality control reviews and maintain databases and project-specific status reports.
Salary not listed
IQVIA
The Study Start-Up CRA is responsible for managing site selection, study-specific start-up activities, and ensuring deliverables are met for Phase I-IV trials. They act as the primary contact for trial sites, facilitating document collection, regulatory submissions, and site greenlight processes.
$71,900 - $145,300 / YEAR
2 months ago
Firelands Health
This role is responsible for overall 340B Program Coordination, including policy development, vendor management, compliance audits, software oversight, and staff education for the health system and associated entities. The coordinator also works with the Director of Pharmacy to strategically expand services, reduce expenses, and improve overall health system margin.
