ICON plc
Bengaluru, Karnataka, India Posted 2d ago
At ICON Strategic Solutions in Bengaluru, you will work in a sponsor-dedicated model designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments. You will manage day-to-day clinical trial management activities supporting your team to deliver quality outcomes.
Key Responsibilities
Lead the planning, execution, and monitoring of complex clinical trials ensuring adherence to regulatory requirements and project timelines.
Collaborate closely with cross-functional teams including investigators, vendors, and internal stakeholders.
Develop and manage comprehensive study plans, budgets, and timelines while optimizing resource utilization.
Spearhead the resolution of intricate issues and challenges arising during clinical trials using strategic problem-solving skills.
Implement and oversee robust monitoring and validation processes ensuring data integrity and quality standards.
Requirements
Bachelor's degree in a relevant scientific discipline or healthcare-related field.
Extensive experience in clinical study management showcasing a grasp of the drug development process and regulatory landscape.
Proven ability in project management, handling multiple tasks concurrently, and prioritizing duties.
Exceptional communication and interpersonal skills fostering collaboration with cross-functional teams.
Detail-oriented with dedication to data accuracy and quality standards.
