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Evolution Research Group
Overview
The Sub-Investigator acts as the secondary physician overseeing clinical trials, ensuring protocol adherence and regulatory compliance at the research site. They are responsible for managing subject care, documenting study procedures, and maintaining the integrity of clinical data.
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Compensation
$100,000 - $150,000 / YEAR
Posted
9 days ago
The US Oncology Network
Responsible for managing research regulatory and administrative activities for clinical trials, including site qualification and document management. Collaborates with investigators and central operations to ensure compliance with SOPs, GCP, and federal regulations.
Salary not listed
24 days ago
Structure Therapeutics
The Senior Clinical Trial Associate supports the planning and implementation of clinical studies by managing study-related documents and the Trial Master File. They act as a central contact for study teams, coordinating with vendors, investigative sites, and cross-functional groups.
$110,000 - $120,000 / YEAR
1 month 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
Flourish Research
The Regulatory Specialist manages and coordinates all regulatory documents and activities for clinical research studies. This includes overseeing submissions to IRBs and sponsors while ensuring compliance with federal regulations and site protocols.
$24 - $29 / HOUR
