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4 C Medical Technologies
Overview
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
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Compensation
$75,000 - $95,000 / YEAR
Posted
6 days ago
VITAS Healthcare
The Coordinator Claims II is responsible for validating services rendered to Vitas patients by checking billed data on claims and invoices against contracted negotiated financial arrangements. This role also involves applying general claims/invoice processing procedures and guidelines for all billed services.
Salary not listed
2 months ago
Spyglass Pharma
The Clinical Project Assistant will support the execution of clinical studies by contributing to the day-to-day operations of clinical trials across all phases of development. This includes assisting in the preparation, organization, and tracking of key clinical and regulatory documents to ensure high-quality trial execution.
$28 - $32 / HOUR
Lifescape Community Services
The Case Manager/Care Coordinator assesses, authorizes, and manages Community Care Program (CCP) services while providing ongoing case management to eligible participants across four counties. This role involves conducting community-based assessments, developing Person-Centered Plans of Care, arranging service implementation with vendors, and ensuring compliance with Illinois Department on Aging regulations.
INSIGHT Surgical Hospital
The ED Utilization Review/Case Manager facilitates appropriate hospital resource use by verifying acute inpatient criteria and assisting with timely discharge needs. This role serves as a central communicator, collaborating with internal and external parties on discharge planning and utilization review activities.
3 months ago
Structure Therapeutics
The Senior Clinical Trial Associate serves as a central contact supporting the clinical study team in planning, implementing, and completing studies by interacting with sites, vendors, and team members. Key duties include obtaining, reviewing, and tracking study documents, setting up and maintaining the Trial Master File (TMF/eTMF), and facilitating meeting preparations.
$110,000 - $120,000 / YEAR
