Study Design and Protocol Development: Creating detailed plans for clinical trials, including objectives, methodology, and timelines.
Site Selection and Management: Identifying and selecting appropriate clinical trial sites, managing relationships with investigators, and overseeing site operations.
Patient Recruitment and Enrollment: Developing strategies to attract and enroll eligible patients into clinical trials.
Data Collection and Management: Collecting, organizing, and managing clinical trial data, ensuring accuracy and completeness.
Monitoring and Auditing: Conducting regular monitoring visits to clinical trial sites to assess compliance with protocols and regulatory requirements.
Project Management and Reporting: Overseeing the overall project timeline, budget, and deliverables, and providing regular progress reports to stakeholders.
