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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
Care Access
Support clinical research events by performing phlebotomy, handling biospecimens, and ensuring accurate documentation. Manage event operations including setup, breakdown, and guiding participants through the research flow.
$19 - $44 / HOUR
8 days ago
This event-based role involves supporting participant care and clinical research event operations, including performing venipuncture, handling biospecimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing event stations, guiding participants through the flow, and maintaining a professional workspace.
$44 / HOUR
This event-based role involves supporting participant care and clinical research event operations, including performing phlebotomy, handling biospecimens, and accurately documenting all procedures according to regulatory standards. Responsibilities also include setting up and managing event stations, ensuring smooth operations, and maintaining compliance and participant safety.
This event-based role involves supporting participant care and clinical research event operations, including performing phlebotomy, handling biospecimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing event stations, guiding participants through the flow, and maintaining a safe, professional workspace.
This event-based role involves supporting participant care and clinical research event operations, including performing phlebotomy, handling specimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing event stations, guiding participants through the flow, and maintaining a safe, compliant workspace.
15 days ago
This event-based role involves supporting participant care and event operations, including performing phlebotomy, handling specimens, and accurately documenting all procedures in paper or electronic systems. Responsibilities also include setting up and managing clinical research events to ensure they run smoothly, safely, and compliantly.
23 days ago
This event-based role involves supporting participant care and clinical research operations, including performing venipuncture, handling biospecimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing clinical research events to ensure smooth, safe, and compliant execution.
This event-based role involves supporting participant care and clinical research operations, including performing venipuncture, handling biospecimens, and ensuring accurate documentation according to regulatory standards. Responsibilities also include setting up and managing clinical research events to ensure smooth, safe, and compliant execution while guiding participants through the process.
The Clinical Research Assistant will support participant care and event operations by performing phlebotomy, handling specimens, and accurately documenting all procedures in compliance with regulations. This role also involves setting up and managing clinical research events to ensure they run smoothly, safely, and professionally.
Labcorp
The Veterinary Technician will support the Veterinarian by performing various animal care procedures, including radiographs and sample collection. They will also assist with surgical requirements and ensure compliance with regulatory guidelines.
$23 - $25 / HOUR
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
1 month ago
BioAgilytix
The Study Coordinator will be responsible for maintaining accurate study records, tracking project samples, and supporting assay quality control testing performed during sample analysis. This role also involves supporting study start-up, end-of-study activities, and maintaining essential documentation like CoAs and reagent records.
Salary not listed
2 months ago
