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AstraZeneca
Overview
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.
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Compensation
Salary not listed
Posted
22 days ago
Alcanza Clinical Research
The Clinical Research Coordinator ensures the execution of assigned studies in compliance with regulations and protocols. Responsibilities include patient screening, data entry, and maintaining communication with clients and team members.
23 days ago
Allina Health
This role involves coordinating high-quality care for patients in clinical research studies by ensuring standards are met, educating participants, and collaborating across disciplines to support safe and effective study outcomes. Key duties include ensuring patient care aligns with the research protocol, performing safety monitoring, conducting patient evaluations, and assisting the investigator with protocol-specific tasks like dose modifications.
$37 - $51 / HOUR
1 month ago
M3USA
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening participants, maintaining documentation, and ensuring compliance with research protocols.
Perelman School of Medicine at the University of Pennsylvania
The Clinical Research Coordinator will participate in and coordinate clinical trials within the Department of Medicine, supporting a diverse group of investigators. Responsibilities include study design, patient recruitment, regulatory compliance, and data management.
$46,500 - $67,046 / YEAR
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.
Medpace, Inc.
The Study Start-Up Coordinator communicates with research sites to collect essential documents for clinical trials and maintains quality reviews of trial documents. They also manage timelines for study start-up and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality reviews of trial documents. They will also manage timelines for study start-up and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality reviews of trial documents. They will also provide guidance to ensure compliance with regulations and develop solutions to regulatory challenges.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality review of trial documents. They will also manage timelines for study start-up through collaboration with internal teams.
IQVIA
The Study Start-Up CRA is responsible for managing site selection, study-specific start-up activities, and ensuring deliverables are met for Phase I-IV trials. They act as the primary contact for trial sites, facilitating document collection, regulatory submissions, and site greenlight processes.
$71,900 - $145,300 / YEAR
2 months ago
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
CenExel
The Study Start-Up Assistant performs routine administrative and clerical tasks such as file organization, preparing reports or correspondence, and providing administrative support to ensure efficient office operations. Essential duties include managing communications, handling information requests, performing general clerical duties, and resolving administrative inquiries.
Participants in the CSA Graduate Program will work on clinical trials for oncology medicines, contributing to the collection and filing of regulatory documents and study site activation. The program includes rotations through various teams to understand their roles in delivering the oncology portfolio.
$85,000 / YEAR
5 months ago
