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Avalo Therapeutics
Overview
The Clinical Trial Associate will support the planning, execution, and delivery of clinical trials in compliance with regulatory standards and internal SOPs. Responsibilities include tracking study progress, managing vendor relationships, and ensuring the quality and completeness of trial documentation.
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Compensation
Salary not listed
Posted
6 days ago
Rapport Therapeutics
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.
$90,000 - $110,000 / YEAR
10 days ago
Crinetics Pharmaceuticals
The CTA supports the study team by executing study activities according to protocols and regulatory guidelines across investigator sites. Key duties include maintaining the Trial Master File, coordinating regulatory documents, and assisting with project management tasks from inception to database lock.
$70,000 - $87,000 / YEAR
21 days ago
Olema Oncology
Provide administrative and operational support to clinical teams for in-house and outsourced trials. Manage study documentation, vendor relationships, and investigator site communications to ensure trial execution.
$110,000 - $120,000 / YEAR
27 days ago
ALX Oncology Inc.
Supports clinical operations by managing the Trial Master File (TMF), coordinating site activation, and tracking study documents. Collaborates with CROs and internal teams to ensure regulatory compliance and efficient trial execution.
$100,000 - $120,000 / YEAR
29 days ago
Vedanta Biosciences
The Senior Clinical Trial Associate serves as a central hub for the clinical study team, supporting the planning, implementation, and wind-down of clinical trials. Key duties include managing the Trial Master File, coordinating with CROs, and tracking study status and enrollment.
$48 - $55 / HOUR
1 month ago
PTC Therapeutics, Inc.
The Contract, Clinical Trial Associate provides clinical study and Trial Master File (TMF) support for clinical operations, assisting Clinical Trial Managers with various activities. Responsibilities include managing clinical documents, ensuring compliance with regulatory requirements, and supporting budget management.
$35 - $47 / HOUR
The Contract, Clinical Trial Associate provides support for clinical study and Trial Master File (TMF) activities, assisting Clinical Trial Managers with study start-up and document management. Responsibilities also include ensuring compliance with regulatory requirements and managing vendor invoices.
Krystal Biotech
The role involves managing clinical trial supplies, monitoring investigative sites for GCP compliance, and maintaining the Trial Master File. Additionally, the associate will train site staff and collaborate with finance to track study budgets and invoices.
Medpace, Inc.
The Clinical Trial Associate supports Trial Master File (TMF) oversight by ensuring all documents meet established quality standards, which involves managing electronic filing systems, tracking, maintaining, and performing quality checks on documents. This role also requires communication with internal associates globally regarding document errors and preparing documents for shipment.
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
2 months ago
Liquidia
This role involves assisting with project start-up activities such as budget development, contract finalization, and grant payments, while also collaborating on study-related materials like informed consent forms and advertising materials. The associate will also oversee, process, and manage clinical project documents, review the work of CROs and vendors, and maintain various study trackers and systems.
Cellectis
The Clinical Trial Associate supports clinical study teams in trial execution and oversight, focusing primarily on document management, trial tracking, and operational support across study start-up, execution, and close-out phases. Key duties include maintaining inspection-ready documentation in the TMF/eTMF and ensuring data accuracy within the CTMS.
$80,000 - $90,000 / YEAR
3 months ago
Structure Therapeutics
The Senior Clinical Trial Associate serves as a central contact supporting the clinical study team in planning, implementing, and completing studies by interacting with sites, vendors, and team members. Key duties include obtaining, reviewing, and tracking study documents, setting up and maintaining the Trial Master File (TMF/eTMF), and facilitating meeting preparations.
