Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
Alliance For MultiSpecialty Research LLC
Overview
The Study Start-up Assistant supports the start-up process by managing regulatory documents, submitting recruitment materials to the IRB, and maintaining study trackers. They ensure all activities comply with FDA regulations and maintain consistent communication with the start-up leadership team.
Quick view →
Compensation
Salary not listed
Posted
11 days ago
OneOncology
The Research Regulatory Coordinator manages regulatory files, IRB submissions, and essential documentation for clinical trials. They coordinate with sponsors and investigators to ensure compliance with regulatory best practices and safety reporting.
16 days ago
Pharmaron
The Clinical Regulatory Associate manages essential clinical trial documentation, IRB submissions, and study start-up activities. They ensure compliance with GCP, GLP, and internal procedures while supporting monitoring visits and study closeout activities.
$50,000 - $54,000 / YEAR
1 month ago
