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Avalo Therapeutics
Overview
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.
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Compensation
Salary not listed
Posted
6 days ago
Terumo
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.
$44,900 - $61,710 / YEAR
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 sites, driving performance, resolving study-related issues, and managing study supplies.
$112,154 - $168,232 / YEAR
11 days ago
Florida Cancer Specialists
The coordinator is responsible for the overall successful implementation and ongoing site management of research studies. They perform research study duties under the medical supervision of the Principal Investigator and research director.
14 days ago
Iterative Health
The Clinical Research Coordinator II manages daily clinical trial activities, including protocol management, patient recruitment, and study visit coordination. They are responsible for ensuring data integrity, maintaining regulatory documentation, and serving as the primary point of contact for study participants.
The Clinical Research Coordinator III is responsible for the successful implementation and ongoing site management of research studies under the supervision of the Principal Investigator. They also provide clinic coverage, mentor new research staff, and assist with assigned research projects.
16 days ago
ICON plc
The Senior Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining data integrity throughout clinical trials. They also collaborate with site staff and investigators to facilitate study conduct and prepare essential study documentation.
17 days ago
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will collaborate with site staff and perform data review to maintain high-quality clinical trial documentation.
You will oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice standards. This involves conducting site visits, collaborating with cross-functional teams, and providing training to site staff to ensure successful trial execution.
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
Theradex Oncology
The Clinical Research Associate will conduct site monitoring visits, including qualification, initiation, routine, and close-out visits to ensure protocol compliance and data integrity. They will also act as a liaison between study sites and the project team while managing site documentation and safety reporting.
$75,000 - $145,000 / YEAR
1 month ago
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.
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.
Shriners Children's
The Clinical Research Coordinator II ensures oversight and compliance of clinical research activities while serving as the primary liaison between participants, investigators, and sponsors. They are responsible for ethically recruiting pediatric subjects, collecting data, and ensuring subject safety and data quality.
$27 - $41 / HOUR
IQVIA
Perform site monitoring and management to ensure study compliance with protocols, regulations, and sponsor requirements. Manage study progress, including regulatory submissions, recruitment tracking, and data integrity verification.
$64,000 - $189,000 / YEAR
Victor
The Administrative Associate provides general office support, including data entry, phone coverage, and file maintenance. They also assist with site-specific administrative functions such as payroll, technical support, and client intake paperwork.
$22 - $30 / HOUR
Fortrea
The CRA will lead and support the Medical Device & Diagnostics team by managing all aspects of study site monitoring, including routine visits and close-outs. They are responsible for ensuring protocol adherence, data integrity, and the protection of study participants through rigorous clinical research standards.
$105,000 - $117,000 / YEAR
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and data integrity. Additionally, you will collaborate with site staff and investigators to facilitate study conduct and maintain high-quality clinical 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
