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Terumo
Overview
The Clinical Research Coordinator provides administrative and operational support to the Clinical Research and Operations department to ensure adherence to study plans and regulatory standards. Responsibilities include managing study documentation, maintaining the electronic trial master file, and coordinating with clinical sites and vendors.
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Compensation
$44,900 - $61,710 / YEAR
Posted
7 days ago
Systimmune
The Senior CRA manages and oversees assigned clinical study sites to guarantee data quality and patient safety, adhering to ICH-GCP guidelines, local regulations, and SOPs. Responsibilities include performing all types of monitoring visits, managing site compliance, assisting in study plan development, and overseeing recruitment strategies.
$90,000 - $130,000 / YEAR
9 days ago
The Study Startup Specialist coordinates and oversees all aspects of clinical trial initiation, including managing essential document collection, regulatory submissions to bodies like IRB/EC, and tracking startup milestones to ensure sites are ready for patient enrollment on time. This role involves preparing, reviewing, and submitting regulatory documents, supporting contract/budget negotiations, and maintaining audit-ready documentation in systems like eTMF.
$70,000 - $95,000 / YEAR
AstraZeneca
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for study sites, driving performance, resolving issues, and ensuring data quality through monitoring visits and source data review.
$112,154 - $168,232 / YEAR
11 days ago
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites, ensuring compliance with guidelines like ICH-GCP and local regulations. This role involves acting as the main contact for sites, driving performance, resolving study-related issues, and managing study supplies.
ICON plc
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data entry and site documentation.
Salary not listed
17 days ago
The Clinical Research Associate serves as the primary point of contact for investigational sites, ensuring compliance with ICH-GCP and regulatory standards. They are responsible for conducting site visits, monitoring patient safety, managing data integrity, and overseeing drug accountability.
The Senior Clinical Research Associate is locally responsible for study delivery at allocated sites, acting as the main contact for monitoring study conduct to ensure compliance with guidelines like ICH-GCP. Responsibilities include performing site visits, driving site performance, resolving study issues proactively, and managing site training and enrollment milestones.
22 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
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.
$110,000 - $120,000 / 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
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
ZOLL Medical Corporation
Provide administrative and operational support for clinical trials, including the maintenance of trial master files and regulatory documentation. Coordinate study activities, manage clinical data in CTMS and EDC systems, and ensure compliance with GCP and SOPs.
$28 - $32 / 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
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting site visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for monitoring patient safety, managing site documentation, and overseeing drug accountability throughout the clinical trial process.
$91,336 - $114,170 / YEAR
The Clinical Research Associate serves as the primary point of contact for investigational sites, ensuring compliance with ICH-GCP and regulatory standards. They are responsible for conducting site visits, monitoring patient safety, managing documentation, and overseeing drug accountability.
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
Alliance for Clinical Trial in Oncology Foundation
The Clinical Research Associate will manage clinical trial operations, including site selection, study start-up, and maintenance of trial master files. They will collaborate with CROs and investigative sites to ensure compliance with ICH GCP guidelines and organizational standards.
2 months ago
Ardelyx
The Clinical Research Associate II provides sponsor oversight of assigned investigative sites, focusing on high-quality protocol execution and compliance with GCP and regulatory requirements. This role involves monitoring site performance through data review, supporting all phases of the clinical trial lifecycle, and ensuring timely collection and maintenance of essential regulatory documents.
$99,000 - $121,000 / YEAR
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
