Develop, coordinate, and implement clinical research studies at the organization's facilities, ensuring adherence to study protocols and timelines
Collaborate with the principal investigator to design study protocols and ensure scientific integrity
Liaise between research subjects, client teams, investigators, and clinic operations teams to facilitate smooth communication and coordination
Plan logistics and resource usage for clinical trials, including scheduling, staffing, and equipment needs
Track study progress in alignment with project milestones, client deliverables, and budget, and provide regular updates to stakeholders
Ensure compliance with applicable regulations globally and by region, including Good Clinical Practice (GCP) guidelines
Supervise experienced support employees and/or entry-level individual contributors, planning, prioritizing, and directing their tasks to ensure efficient workflow and high-quality output
Deliver operational results that have a moderate impact on the immediate achievement of results for the team, contributing to the overall success of the organization
Adapt new procedures, techniques, and tools to improve clinical trial processes and outcomes
Understand basic management approaches such as work scheduling, prioritizing, coaching, and process execution
Requirements
Broad job knowledge in an operational, administrative, and/or specialized field
Practical knowledge in managing the execution of processes, projects, and tactics within a team
Understanding of the impact of work on related areas
Relevant certifications in clinical trial management or related fields
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