The Clinical Trial Assistant coordinates study activities, manages study documentation, and facilitates communication between internal teams and external stakeholders. They also provide technical support for the company portal and handle administrative tasks such as invoicing and survey management.
The Proposal Analyst I is responsible for creating accurate and timely proposal estimates for patient travel and reimbursement services. This role involves collaborating with cross-functional teams and ensuring all deliverables align with client requirements and internal standards.
The Compliance Administrator supports quality, regulatory affairs, and vendor management by ensuring adherence to statutory and regulatory standards. Responsibilities include managing quality assessments, vendor onboarding, contract tracking, and maintaining regulatory documentation.
The Manager of Site Strategy and Engagement is responsible for building and maintaining strong relationships with clinical research sites to ensure successful engagement and performance throughout the clinical trial lifecycle. They will monitor site utilization, resolve operational issues, and provide regional expertise to support client needs and marketing efforts.
