Clinical Trial Delivery Lead

Regulatory Jobs; Center Square (PA); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Employee assistance programmes

Learning and development opportunities

Job summary

ICON Strategic Solutions is seeking a Clinical Study Manager to oversee the design, execution and analysis of clinical trials. You will coordinate cross-functional teams, ensure regulatory compliance, and drive study timelines to deliver high-quality data that supports patient outcomes.

The role emphasizes strong project management, collaboration with investigators and vendors, and meticulous attention to data integrity across the study lifecycle.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Proven experience in clinical study management with understanding of drug development and regulatory requirements.
• Excellent project management skills with ability to handle multiple tasks and priorities.
• Strong communication and interpersonal skills for cross-functional collaboration with investigators, vendors and partners.
• Detail-oriented with focus on data accuracy and high-quality trial standards.

Responsibilities

• Oversee planning, execution, and monitoring of clinical trials to ensure regulatory compliance and timelines.
• Collaborate with investigators, vendors, and internal stakeholders to drive study implementations.
• Develop and manage study budgets, resources, and timelines to optimize study plans.
• Lead resolution of issues during trials with effective problem-solving and communication.
• Ensure data integrity and quality through monitoring and validation throughout the study lifecycle.

Skills

Project management

Cross-functional collaboration

Data integrity

Communication

Clinical trial management

Education

Bachelor's degree in science

Job description

ICON Strategic Solutions is seeking a Clinical Study Manager to oversee the design, execution and analysis of clinical trials. You will coordinate cross-functional teams, ensure regulatory compliance, and drive study timelines to deliver high-quality data that supports patient outcomes.

The role emphasizes strong project management, collaboration with investigators and vendors, and meticulous attention to data integrity across the study lifecycle.