Clinical Trial Manager at ICON managing trial operations, ensuring high - quality outcomes and compliance with trial protocols for clinical development in Beijing and Shanghai.
About the role
- Principal Clinical Study Manager leading planning and execution of clinical studies at Stryker. Collaborating with teams to ensure compliance and operational excellence in stroke care.
Responsibilities
- Lead the planning and execution of complex clinical studies that advance innovation in stroke care
- Collaborate with cross-functional teams
- Ensure compliance with regulatory standards
- Drive operational excellence to deliver high-quality results
- Define and manage program scope
- Develop and maintain a comprehensive program schedule
- Create and manage program budgets
- Partner with project teams to develop Quality Plans
- Establish and execute a risk management plan
- Develop a Procurement Management Plan
Requirements
- Bachelor’s degree
- 8+ years of relevant work experience in program or project management
- Proven ability to manage complex programs, budgets, schedules, and cross-functional teams
- Strong leadership, communication, and stakeholder management skills
- Preferred MS or MBA
- PMP, PgMP, or equivalent professional certification
- Experience in procurement planning and vendor management
- Familiarity with quality systems and risk management methodologies
Benefits
- salary plus bonus eligible
- benefits
Job title
Job type
Experience level
Salary
Degree requirement
Tech skills
Location requirements
Clinical Research Coordinator overseeing research studies at Florida Cancer Specialists. Responsible for implementation and management of clinical trials under medical supervision.
Senior Clinical Trial Manager at Climb Bio leading end - to - end execution of Phase 1 - 3 clinical studies. Critical role in clinical operations and study management with a focus on quality and compliance.
Senior Clinical Researcher collaborating globally to design and evaluate digital health investigations. Engaging in statistical analysis and contributing to product development for cognitive health.
Assistente de Pesquisa Clínica Júnior supporting scientific team for clinical studies and protocol development at MEDCIN Pesquisa Clínica.
Clinical Research Project Coordinator providing research project support across Intermountain system. Responsible for project coordination, communication, and documentation in healthcare research.
Principal Biostatistician Consultant at ClinChoice overseeing drug development statistical methodologies. Lead statistician for clinical studies in a hybrid work environment.
Part - time Clinical Research Coordinator for Penn's Center for Weight and Eating Disorders. Assist in industry - funded study on behavioral treatment effects and weight loss medications.
Clinical Research Coordinator supporting clinical research at University of Wisconsin. Collaborating with investigators and multidisciplinary teams to advance patient - centered research.
Managing clinical research coordinators for data quality and participant management at USF Health. Overseeing daily operations and coordinating with sponsors, ensuring compliance in clinical trials.