Responsibilities
- Oversee biomarker studies within clinical trials while adhering to regulatory standards
- Provide operational expertise during quote and proposal development to align service capabilities with client requirements
- Review project scope and financial plans to consistently meet client expectations
- Establish key project milestones and monitor progress from contract signing to final payment
- Ensure projects follow established global procedures and quality standards
- Manage and track budgets for assigned studies
- Maintain precise and complete study documentation to support regulatory audits
- Assist in sponsor-led and internal audit processes
Work Arrangement
Remote (City/Region)
Other
Informal and pleasant working environment
