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Neurocrine Biosciences
Overview
Supports operational activities for the planning, initiation, conduct, and close-out of domestic and global clinical studies. Manages essential document collection, IRB/IEC submissions, and ensures compliance with GCP and regulatory standards.
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Compensation
$89,800 - $123,000 / YEAR
Posted
15 days ago
Quest Diagnostics
Ensures the laboratory maintains constant inspection readiness. Manages quality assurance processes within the clinical lab environment.
$46 - $68 / HOUR
16 days ago
AstraZeneca
Field Clinical Advisors are crucial for the successful execution of cell therapy clinical trials by driving recruitment, retention, and safety management while generating early insights. They focus on clinical study protocol expertise, educating sites, optimizing the patient journey, and engaging with the cell therapy pipeline.
$197,000 - $295,000 / YEAR
1 month ago
Vericel Corporation
The TMF Specialist manages the end-to-end quality and integrity of clinical trial documentation to ensure continuous inspection readiness. This includes developing TMF plans, resolving documentation gaps, and supporting CRAs with site file reconciliations.
$75,000 - $95,000 / YEAR
Prime Medicine
The role involves supporting clinical trial execution from startup through closeout, including site activation, regulatory documentation, and TMF oversight. You will also coordinate with internal teams, CROs, and clinical sites to ensure protocol compliance, data integrity, and timely issue resolution.
$117,000 - $143,000 / YEAR
Cell Therapy Field Clinical Advisors are crucial for the successful execution of clinical trials by driving recruitment, retention, and safety management, while also providing early insight generation. They focus on clinical study protocol expertise, educating sites, optimizing the patient journey, and engaging with the cell therapy pipeline.
Dyne Therapeutics
The Senior TMF Specialist is responsible for the maintenance, quality, and inspection readiness of the Trial Master File across assigned clinical studies. This role involves collaborating with cross-functional teams and vendors to ensure document integrity and compliance with regulatory standards.
$155,000 - $190,000 / YEAR
Medpace, Inc.
The associate will manage sponsor audits and regulatory inspections (FDA, EMA, MHRA), facilitate QA relationships with external clients, and conduct inspection readiness activities for Medpace stakeholders. Key duties include facilitating onsite audits, reviewing audit responses, managing inspection backrooms, and providing guidance to study teams during inspections.
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