This is a fully remote position, open to applicants in Ohio, +2 more states.

📋 Description

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

• Ensure adherence to protocols, data integrity, and patient safety throughout the trial process.

• Collaborate with investigators and site personnel to facilitate seamless study execution.

• Conduct data reviews and resolve queries to uphold high-quality clinical data standards.

• Assist in the preparation and evaluation of study documentation, including protocols and clinical study reports.

• Operate within a sponsor-dedicated model, enhanced by ICON’s global expertise.

⛳️ Requirements

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

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

• Oncology monitoring experience is mandatory.

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

• Excellent organizational and communication abilities, with a keen attention to detail.

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

• Willingness to travel as needed, up to 50% within the Northeast region.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Learning and development opportunities through structured training and career pathways.