Clinical Trial Program Delivery Lead

ICON; Center Square (PA); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Global Employee Assistance Programme

Life assurance

Flexible benefits

Job summary

ICON plc is a global leader in healthcare intelligence and clinical research. As a CRA II, you will design and analyze clinical trials, ensuring data integrity and patient safety across study activities.

You will conduct site visits, coordinate with investigators, and review data to support high-quality outcomes. Travel up to 60% is required, with opportunities for professional growth and competitive benefits.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• Knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%)

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Skills

Clinical trial monitoring

ICH-GCP

Regulatory knowledge

Data integrity

Communication skills

Travel readiness

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

ICON plc is a global leader in healthcare intelligence and clinical research. As a CRA II, you will design and analyze clinical trials, ensuring data integrity and patient safety across study activities.

You will conduct site visits, coordinate with investigators, and review data to support high-quality outcomes. Travel up to 60% is required, with opportunities for professional growth and competitive benefits.