Clinical Research

• Develop and coordinate Phase 1 clinical research studies, ensuring all aspects of the study are meticulously planned and executed
• Implement clinical research protocols and ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines
• Collaborate with principal investigators, research subjects, client teams, and clinic operations teams to facilitate smooth communication and coordination
• Plan and manage logistics and resource usage for clinical trials, including scheduling, budgeting, and resource allocation
• Track study progress and ensure alignment with project milestones, client deliverables, and budget, providing regular updates to stakeholders
• Prepare and present study reports and updates to stakeholders, including detailed analysis of study data and progress
• Ensure adherence to global and regional regulations and guidelines, staying up-to-date with any changes or updates
• Provide guidance and support to lower-level professionals and team members, fostering a collaborative and supportive work environment
• Identify and resolve any issues or challenges that arise during the course of the study, ensuring timely and effective solutions
• Maintain accurate and comprehensive documentation of all study-related activities, ensuring transparency and accountability

Clinical Trial Manager I

Single Sponsor Clinical Trial Manager I