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ICON plcNew
Overview
The intern will support clinical delivery by managing essential document collection, maintaining the Trial Master File, and ensuring timely data entry into CTMS. They will also assist with risk assessment, trial material tracking, and general clinical operations tasks.
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Compensation
$19 / HOUR
Posted
New
ICON plc
The Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.
$110,520 - $138,150 / YEAR
2 days ago
Avalo Therapeutics
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.
Salary not listed
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
11 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
Neurocrine Biosciences
Supports Clinical Operations by managing the quality, compliance, and inspection-readiness of Trial Master Files (TMF). Acts as a subject matter expert for eTMF systems, facilitating audits and collaborating with cross-functional teams to maintain study documentation.
$89,800 - $123,000 / YEAR
24 days ago
Thermo Fisher Scientific
The Clinical Trial Coordinator supports the planning and execution of clinical studies, focusing on day-to-day activities and regulatory inspection readiness. They collaborate with study teams, CROs, and internal departments to manage study documentation and clinical trial systems.
27 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
Structure Therapeutics
The Senior Clinical Trial Associate supports the planning and implementation of clinical studies by managing study-related documents and the Trial Master File. They act as a central contact for study teams, coordinating with vendors, investigative sites, and cross-functional groups.
1 month ago
Liquidia
The TMF Associate ensures the Trial Master File is complete, inspection-ready, and compliant with regulatory requirements and SOPs. This includes performing health checks, managing documentation flow with CROs, and supporting internal and regulatory audits.
Syneos Health
Coordinate and manage clinical research projects, including site preparation, patient recruitment, and data collection. Ensure all study activities comply with Good Clinical Practices (GCP) and regulatory requirements while supporting the Principal Investigator.
$49 - $59 / HOUR
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-down. Ensure compliance with regulatory requirements, informed consent, and safety reporting through remote and on-site monitoring.
Manage research activities at clinical sites, including site identification, start-up, and close-down processes. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
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
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
Coordinate and manage clinical research projects, including site start-up, patient recruitment, and data collection. Ensure all study activities comply with Good Clinical Practices (GCP) and regulatory requirements while supporting the Principal Investigator.
GRAIL
The Clinical Project Assistant supports study teams in Clinical Operations by managing administrative aspects of clinical trial execution. Key duties include maintaining the Trial Master File, tracking site payments, and assisting with quality metrics and meeting coordination.
$33 - $39 / HOUR
Pathos
The role focuses on maintaining the Trial Master File and coordinating operational workflows between sites, CROs, and vendors to ensure inspection-ready FDA submissions. Additionally, the position involves identifying opportunities to automate clinical workflows using AI systems to accelerate trial timelines.
$75,000 - $85,000 / YEAR
Caris Life Sciences
Provide operational and regulatory support for sponsored and collaborative pharma studies, focusing on site onboarding and engagement. Manage study documentation, specimen tracking, and inventory while ensuring compliance with SOPs.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Ensure compliance with informed consent, safety reporting, and regulatory requirements through remote and on-site monitoring.
