Clinical Research Associate

This is a fully remote position, open to applicants in Connecticut, +3 more states.

📋 Description

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

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

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

• Perform data reviews and address queries to uphold the quality of clinical data.

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

• Assume responsibility for clinical trial monitoring deliverables and foster collaborative efforts.

⛳️ Requirements

• 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.

• Experience in monitoring Ophthalmology trials or multi-Therapeutic Area (TA) studies.

• Strong organizational and communication skills, with a keen attention to detail.

• Ability to work independently as well as collaboratively in a dynamic environment.

• Willingness to travel as necessary, approximately 60% of the time.

• Legal eligibility 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 plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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