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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
10 days ago
Lilly
Design and execute in vitro and ex vivo studies to advance priority oncology targets through the drug discovery pipeline. Develop and validate bioanalytical assays while managing external collaborations and presenting findings to stakeholders.
$71,250 - $187,000 / YEAR
13 days ago
Helmsley
Provide comprehensive administrative support to the Type 1 Diabetes team, including calendar management, travel arrangements, and expense reporting. Coordinate logistics for meetings and serve as the primary point of contact for vendors, contractors, and grantees.
$73,000 - $81,100 / YEAR
Saint Luke's Health System
The Charge Audit Specialist supports charging accuracy among clinical departments and serves as a liaison between clinical and Patient Accounts departments. They manage work queues, assist with charge correction projects, and collaborate with various departments for charge issue resolution.
25 days ago
Johns Hopkins University
Develop and validate assays and protocols while designing experimental approaches for laboratory projects. Responsible for troubleshooting, training new personnel, and contributing to scientific manuscripts and proposals.
$41,300 - $72,300 / YEAR
28 days ago
Children's Healthcare of Atlanta
The Executive Assistant provides executive-level administrative support for the Executive Team, including managing calendars, scheduling meetings, and coordinating logistics. Additional responsibilities include processing invoices, maintaining payroll reports, and supporting project consultants and managers.
29 days ago
Excelsia Injury Care
The role involves managing daily administrative tasks including payroll punch reviews, office supply procurement, and payment processing. Additionally, the assistant coordinates with external vendors and provides general support to managers for special projects and events.
1 month ago
Prime Medicine
The role involves supporting clinical trial execution from startup through closeout, including site activation, regulatory documentation, and TMF oversight. You will also coordinate with internal teams, CROs, and clinical sites to ensure protocol compliance, data integrity, and timely issue resolution.
$117,000 - $143,000 / YEAR
American Addiction Centers
Coordinate instrument repairs, manage vendor loaner sets, and maintain accurate tracking logs for surgical instrumentation. Ensure instrument availability for surgical cases while managing inventory levels and supporting departmental budget goals.
$23 - $34 / HOUR
Profound Research
The Clinical Research Coordinator manages all clinical trial activities, including study start-up, subject recruitment, and data collection in compliance with protocols and regulations. They also mentor staff and ensure accurate documentation and reporting of adverse events.
CenExel
The Clinical Research Coordinator is responsible for managing all aspects of clinical trials, including patient involvement, data collection, and regulatory compliance. They also assist with site operations, vendor oversight, and the education of study participants regarding protocol expectations.
The Clinical Research Coordinator manages all clinical trial activities, including study start-up, subject recruitment, and data collection in compliance with protocols. They also mentor staff and ensure accurate documentation and reporting of adverse events.
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
The Clinical Research Coordinator manages all clinical trial activities in compliance with study protocols, regulations, and company standards. They are responsible for subject recruitment, data collection, regulatory documentation, and mentoring staff to ensure high-quality clinical research operations.
The Clinical Research Coordinator manages patient involvement and study data in strict adherence to ICH and GCP guidelines. They also assist with regulatory duties, safety assessments, and provide support to the Clinical Trial Manager.
2 months ago
The Clinical Research Coordinator manages all clinical trial activities in compliance with research protocols, regulations, and company standards. They are responsible for subject recruitment, data collection, regulatory documentation, and mentoring staff to ensure high-quality clinical trial conduct.
JENAVALVE TECHNOLOGY INC
The Clinical Research Associate supports the conduct of pre-market and post-market clinical studies while ensuring compliance with regulatory requirements. Responsibilities include managing trial documentation, performing data quality checks, and coordinating with site staff and investigators.
$75,000 / YEAR
The Senior Clinical Research Associate will support the conduct of pre-market clinical studies, ensuring compliance with regulatory requirements, and will manage data collection, query resolution, and status reporting for clinical staff and management. Responsibilities also include conducting EDC training, maintaining Trial Master Files, managing regulatory documents, and supporting clinical audits.
$95,000 / YEAR
The Clinical Research Associate will proactively support the conduct of pre-market and/or post-market clinical studies, ensuring compliance with all regulatory requirements under the Director of Clinical Affairs. Key duties include supporting site management, ensuring quality data management, maintaining trial documentation, and conducting internal file audits for compliance.
Firelands Health
This role is responsible for overall 340B Program Coordination, including policy development, vendor management, compliance audits, software oversight, and staff education for the health system and associated entities. The coordinator also works with the Director of Pharmacy to strategically expand services, reduce expenses, and improve overall health system margin.
3 months ago
