Job Description & How to Apply Below
As part of the clinical study operations team, you will guide local study teams to ensure the timely execution of trials in line with regulatory standards. Manage all aspects of site activities, including feasibility assessments, oversight, and close-out operations, while maintaining essential relationships with investigators and stakeholders. Your leadership will enhance operational efficiency and support patient care initiatives.
Key Responsibilities:
• Lead local teams to ensure timely trial delivery
• Manage site selection and monitoring activities
• Ensure compliance with ICH-GCP and sponsor criteria
• Maintain accurate documentation in trial management systems
• Develop and track risk management strategies
Requirements:
• Minimum of 3 years in clinical development roles
• Strong familiarity with ICH-GCP guidelines
• Proven ability to manage complex operations
• Excellent communication and relationship-building skills
• Bachelor’s degree in relevant life sciences field
Facilitate impactful clinical development efforts that contribute to the healthcare landscape.
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Position Requirements
10+ Years
work experience
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