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IQVIA
Overview
The Research Coordinator ensures effective conduct of clinical trials by advocating for patient safety, maintaining protocol integrity, and overseeing patient screening and study requirements. Responsibilities include adhering to federal/institutional regulations, managing informed consent processes, and coordinating all protocol-required patient events.
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Compensation
$43,400 - $108,200 / YEAR
Posted
2 days ago
Systimmune
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
$90,000 - $130,000 / YEAR
10 days ago
The CRA II manages and oversees clinical study sites to ensure data quality and patient safety in compliance with ICH-GCP and local regulations. Key duties include performing site visits, managing patient recruitment, and maintaining the Trial Master File.
$80,000 - $110,000 / YEAR
23 days ago
Caris Life Sciences
Provide operational and regulatory support for sponsored and collaborative pharma studies, focusing on site onboarding and engagement. Manage study documentation, specimen tracking, and inventory while ensuring compliance with SOPs.
Salary not listed
1 month ago
