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IQVIA
Overview
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
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Compensation
$71,900 - $169,300 / YEAR
Posted
9 days ago
Headlands Research
Coordinate all aspects of assigned clinical trials from site initiation through close-out, ensuring compliance with protocols and regulatory standards. Manage subject visits, recruitment, data entry, and collaboration with investigators and sponsors.
$70,000 - $80,000 / YEAR
10 days ago
The Clinical Research Coordinator manages and executes Phase I-IV clinical studies while ensuring compliance with FDA regulations and GCP/ICH guidelines. Responsibilities include subject recruitment, data entry, documentation, and collaboration with investigators and sponsors.
Salary not listed
ICON plc
You will conduct clinical trial monitoring activities, including site visits and data review to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while contributing to the preparation of essential study documentation.
17 days ago
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.
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.
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
1 month ago
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
Hawthorne Health
Assist the Principal Investigator in overseeing clinical trials while ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all study-related data.
$150 / HOUR
Assist the Principal Investigator in managing clinical trials while ensuring adherence to study protocols and regulatory requirements. Provide medical oversight for study participants and maintain accurate documentation of all clinical trial data.
The Clinical Research Associate performs site monitoring visits to ensure study protocols, regulations, and sponsor requirements are strictly followed. They manage site progress, including recruitment, data integrity, and regulatory documentation to ensure high-quality study execution.
$71,900 - $189,000 / YEAR
The Clinical Research Associate will monitor and manage clinical trial sites to ensure strict adherence to study protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, overseeing recruitment plans, managing documentation, and providing training to site staff.
CenExel
The Quality Assurance Coordinator ensures data quality and participant safety by monitoring adherence to study protocols, SOPs, and federal regulations. They assist in developing QA programs, perform documentation reviews, and prepare the site for internal and external audits.
The Senior CRA is responsible for monitoring and managing clinical sites to ensure strict adherence to study protocols, regulatory requirements, and sponsor expectations. They will conduct various site visits, facilitate subject recruitment, and maintain essential study documentation to ensure high-quality clinical research data.
$87,200 - $169,300 / YEAR
Flourish Research
The Clinical Research Coordinator assists investigators in executing clinical trials in accordance with study protocols and regulatory guidelines. Responsibilities include obtaining informed consent, performing lab draws, managing study documentation, and communicating with sponsors.
$24 - $26 / HOUR
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.
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
2 months ago
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
Ann & Robert H. Lurie Children's Hospital of Chicago
This role coordinates all aspects of clinical research projects, overseeing activities from study start-up through close-out while ensuring strict adherence to protocols and regulatory requirements. Key functions include managing regulatory documentation, participant engagement, data lifecycle management, and assisting with financial and dissemination activities.
$59,280 - $96,928 / YEAR
University of Texas at Austin
The Clinical Research Associate I will manage and oversee the day-to-day coordination and operations of assigned clinical research projects, focusing significantly on recruitment, enrollment, and research activities within the Department of Psychiatry. Key duties involve assisting in the planning, execution, and monitoring of clinical trials to ensure strict compliance with regulatory requirements and study protocols, including site management and data integrity.
$40,000 / YEAR
3 months ago
