Senior Clinical Trial Manager

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

Benefits offered by this job

Competitive base salary

Performance incentives

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Learning and development opportunities

Job summary

ICON Strategic Solutions’ Clinical Trial Manager II role focuses on designing and analyzing trials within a sponsor-dedicated model. You’ll oversee workstreams, ensure quality and timelines, and contribute to the advancement of treatments.

The role emphasizes regulatory compliance and stakeholder collaboration across teams. Qualified candidates bring 5+ years in trial management, strong data interpretation skills, and the ability to travel about 10%.

Qualifications

• Bachelor's degree in a relevant field with at least 5 years in clinical trial management.
• Proven expertise in designing and executing clinical trials with regulatory understanding.
• Analytical and problem solving skills for complex medical data interpretation.
• Effective communication and collaboration across diverse teams.
• Detail oriented and able to manage multiple priorities simultaneously.
• Willingness to travel approximately 10%.

Responsibilities

• Oversee clinical trial management workstreams to meet quality and timelines.
• Collaborate with cross functional teams to design and implement trial protocols.
• Oversee day-to-day trial operations ensuring regulatory compliance.
• Analyze trial data, identify trends and provide insights to improve outcomes.
• Proactively address challenges and communicate with stakeholders to ensure smooth trials.

Skills

Clinical trial management

Regulatory knowledge

Data analysis

Cross-functional collaboration

Project management

Travel willingness

Education

Bachelor's degree in a relevant field

Job description

ICON Strategic Solutions’ Clinical Trial Manager II role focuses on designing and analyzing trials within a sponsor-dedicated model. You’ll oversee workstreams, ensure quality and timelines, and contribute to the advancement of treatments.

The role emphasizes regulatory compliance and stakeholder collaboration across teams. Qualified candidates bring 5+ years in trial management, strong data interpretation skills, and the ability to travel about 10%.