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Rapport Therapeutics
Overview
The Senior Clinical Trial Associate manages clinical study documentation, including the Trial Master File, to ensure inspection readiness and compliance with ICH-GCP standards. They also support the trial team with administrative tasks, vendor invoice tracking, and the preparation of essential study-related documents.
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Compensation
$90,000 - $110,000 / YEAR
Posted
11 days ago
University of Rochester
The specialist is responsible for the coordination and oversight of regulatory requirements for clinical research protocols. They manage documentation, maintain logs in tracking systems, and act as a liaison between study teams, sponsors, and regulatory committees.
$25 - $35 / HOUR
1 month ago
K2 Staffing LLC
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and ongoing reporting. They also collaborate with clinical operations, sponsors, and IRBs to ensure audit-ready regulatory files and compliance with study protocols.
Salary not listed
2 months ago
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and close-out procedures. They also collaborate with clinical operations and sponsors to ensure audit-ready regulatory files and compliance with protocol requirements.
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
The Senior CRA, Field Monitor will participate in clinical research teams to ensure efficient study conduct by providing training, protocol interpretation, document collection/review, and overall clinical trial support. Essential functions include developing training materials, serving as a Subject Matter Expert, overseeing document collection, reviewing data, and training site personnel and vendors on study requirements.
$62 - $67 / HOUR
Structure Therapeutics
The Sr. CRA will independently manage clinical aspects of studies, ensuring adherence to GCPs, SOPs, and protocols while working closely with cross-functional teams, vendors, and sites. Key duties include overseeing study execution from start-up to closeout, managing vendor deliverables, and acting as a point of escalation for site management and CRO monitoring activities.
$135,000 - $150,000 / YEAR
3 months ago
