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ICON plc
Overview
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.
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Compensation
$110,520 - $138,150 / YEAR
Posted
2 days ago
State of Vermont
Registered nurses function as integrated members of a multidisciplinary team to provide high-quality psychiatric nursing care. They contribute to the facility's mission of promoting mental health and well-being through prevention, early intervention, and recovery-focused support.
Salary not listed
7 days ago
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
AHMC Healthcare
Responsible for maintaining the Laboratory Information System (LIS) and performing clinical laboratory testing on patient and control samples. Ensures quality standards, regulatory compliance, and the maintenance of departmental policy and procedure manuals.
$55 / HOUR
21 days ago
Gabrail Cancer Center Research
The Clinical Research Coordinator manages the day-to-day execution of oncology clinical trials, ensuring participant safety and high-quality documentation. Responsibilities include screening participants, conducting study visits, and maintaining regulatory compliance in accordance with GCP and FDA guidelines.
1 month ago
Arizona Liver Health
The Clinical Research Coordinator manages the conduct of clinical trials by implementing protocols, recruiting participants, and ensuring compliance with regulatory standards. They are responsible for collecting and recording research data, performing clinical assessments, and maintaining study documentation.
$28 - $36 / HOUR
Medpace, Inc.
The associate will manage sponsor audits and regulatory inspections (FDA, EMA, MHRA), facilitate QA relationships with external clients, and conduct inspection readiness activities for Medpace stakeholders. Key duties include facilitating onsite audits, reviewing audit responses, managing inspection backrooms, and providing guidance to study teams during inspections.
The Clinical Research Coordinator manages the conduct of clinical research protocols in compliance with FDA, GCP, and company standards. Responsibilities include patient recruitment, data collection, study documentation, and ensuring the safety and well-being of research participants.
2 months ago
Maze Therapeutics
This role involves managing the day-to-day activities for Document Control and GxP Training programs, ensuring processes are completed accurately and on time through cross-functional collaboration. Key duties include managing the full document lifecycle, administering training within the LMS (ComplianceWire), and supporting broader quality system activities.
3 months ago
