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ICON plc
Overview
The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.
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Compensation
Salary not listed
Posted
21 days ago
Minneapolis heart institute foundation
The Research Scholar will conduct clinical research studies related to coronary artery disease and participate in the development and execution of ongoing trials. Responsibilities include evaluating treatment strategies, analyzing data, and contributing to scientific work.
$56,368 / YEAR
2 months ago
Prometrika LLC
The Clinical Trial Associate supports, coordinates, and implements clinical research projects under general supervision. Responsibilities include assisting with study start-up, maintaining study documentation, and ensuring compliance with clinical study standards.
$60,000 - $75,000 / YEAR
ImmunityBio, Inc.
The Field Monitor will support clinical research teams by providing training, interpreting protocols, collecting and reviewing documents, and ensuring the efficient conduct of clinical studies. Key functions include developing training materials, serving as a Subject Matter Expert for sites, overseeing essential document collection, and managing investigational product supply.
$54 - $60 / HOUR
Veristat
The Senior Medical Writer independently plans and prepares regulatory documents and medical communications to support product development phases. They are responsible for organizing, analyzing, and presenting scientific and statistical data in compliance with ICH and company standards.
4 months ago
