In-House Clinical Research Associate

Responsibilities: for the In-House Clinical Research Associate: · Review and manage project documentation to ensure accuracy, completeness, and compliance. · Coordinate with sites and stakeholders to obtain missing information and resolve documentation-related inquiries. · Maintain organized electronic records, files, and tracking systems throughout the project lifecycle. · Monitor document status and workflow progress within centralized databases and internal platforms. · Support administrative and operational processes through accurate recordkeeping and data management. Qualifications: for the In-House Clinical Research Associate: · 3-5 years of clinical research experience, including document management and electronic systems support. · Experience reviewing and maintaining regulatory documentation in a sponsor, CRO, research, or healthcare setting. · Knowledge of clinical research regulations, compliance requirements, and documentation practices. · Experience supporting IRB submissions or regulatory review processes preferred. · Bachelor's degree in a science, health-related, or similar field. Compensation: for the In-House Clinical Research Associate: Salary range: $50,000-80,000 based on professional experience Comprehensive Benefits: Medical, Dental, Vision, 401K, and Sick Leave as required by law