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

Bachelor's degree in a related field (e.g., life sciences, clinical research)
Minimum of 3 years of experience in clinical trial management or a related field
In-depth knowledge of clinical research processes and regulations
Strong project management and organizational skills
Excellent communication and interpersonal skills
Ability to work independently and as part of a team
Proficiency in using clinical trial management software and tools
Certified Clinical Research Professional (CCRP) or equivalent certification preferred

Clinical Trial Manager

Key skills