Clinical Research Associate

This is a fully remote position, open to applicants in Pennsylvania.

📋 Description

• Participate in clinical trial monitoring activities, taking ownership of deliverables and collaborating effectively.

• Execute site qualification, initiation, monitoring, and close-out visits for clinical trials.

• Safeguard protocol adherence, data integrity, and patient safety throughout the trial phases.

• Work alongside investigators and site personnel to ensure smooth study execution.

• Conduct data evaluations and resolve queries to uphold the quality of clinical data.

• Assist in the preparation and examination of study documentation, which includes protocols and clinical study reports.

• Design and evaluate clinical trials, interpret intricate medical data, and aid in the advancement of innovative treatments and therapies.

⛳️ Requirements

• A Bachelor’s degree in a scientific or healthcare-related discipline.

• At least 2 years of experience as a Clinical Research Associate.

• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication skills, with a strong attention to detail.

• Capability to work both independently and collaboratively in a dynamic environment.

• Flexibility to travel as needed (approximately 60%).

• Employment with ICON is subject to having the legal right to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.