The University of Texas MD Anderson Cancer Center
Grifols Shared Services North America, Inc
Grifols Shared Services North America, Inc
Grifols Shared Services North America, Inc
Grifols Shared Services North America, Inc
Grifols Shared Services North America, Inc
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Grifols Shared Services North America, Inc
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Grifols Shared Services North America, Inc
Grifols Shared Services North America, Inc
Grifols Shared Services North America, Inc
Grifols Shared Services North America, Inc
Grifols Shared Services North America, Inc
A leading cancer research institution is seeking a Clinical Trial Associate to assist in study execution activities. This remote position requires a bachelor's degree preference and at least three years of experience in clinical development within the pharmaceutical or biotechnology industry. Ideal candidates will have knowledge of FDA regulations and ICH GCP guidelines. Responsibilities include oversight of CROs, creation of study materials, and coordination with stakeholders.
Job Title: Clinical Trial Associate
Job Number: 37242
Location: Remote
Assists the Clinical Trial Manager with essential study execution activities, including coordination and communication with a wide range of internal and external stakeholders.
Creates study-specific materials such as training presentations, document templates (e.g., training logs), and study newsletters.
Provides oversight of CROs and vendors, including review of the electronic Trial Master File (eTMF) and monitoring visit reports.
Reviews and updates study documentation (e.g., study plans, tracking tools, and site-related documents) to ensure accuracy and completeness.
Develops and maintains detailed study tracking tools to support trial execution, enhance visibility into study progress, and enable effective cross-functional communication.
Supports Clinical Operations administrative activities, including coordinating legal review of contracts and processing purchase order (PO) requests.
A bachelor’s degree is preferred; a background in a scientific or healthcare-related field is desirable but not mandatory.
At least three years of experience in clinical development within the pharmaceutical or biotechnology industry.
Strong understanding of FDA regulations and ICH Good Clinical Practice (GCP) guidelines to support compliant global clinical trial conduct.
Prior experience with clinical trial monitoring and/or conducting site qualification, initiation, interim monitoring, and close-out visits is preferred but not required.
Experience in Alzheimer’s Disease and/or gene therapy will be favorably considered.
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.