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Job Description & How to Apply Below
Elevate clinical study delivery as the Local Study Associate Director at Parexel, ensuring quality and compliance in clinical trials. Lead Local Study Teams to achieve project success.
In this role, you will take charge of overseeing Local Study Teams and managing the lifecycle of clinical trials. Your responsibilities will include the selection of study sites, compliance with regulatory requirements, and effective communication with investigators and stakeholders to ensure successful study execution.
Key Responsibilities:
• Lead and optimize the performance of Local Study Teams
• Evaluate and select potential clinical study sites
• Ensure compliance with ICH-GCP and local laws
• Monitor study data quality and timely reporting
• Facilitate regular team meetings and training sessions
Requirements:
• At least 3 years of experience in clinical development roles
• Strong organizational and detail-oriented skills
• Proficiency in project management principles
• Familiarity with clinical study processes and drug handling
• Fluent in English with knowledge of local languages preferred
Drive the clinical research agenda forward while ensuring engagement and compliance within your Local Study Teams at Parexel.
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