Clinical Research Associate

This is a fully remote position, open to applicants in Connecticut, +8 more states.

📋 Description

• Perform 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.

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

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

• Operate within a sponsor-dedicated model, supporting diverse therapeutic areas.

⛳️ Requirements

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

• At least 1 year of experience in the role of Clinical Research Associate.

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

• Excellent organizational and communication abilities, with a keen eye for detail.

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

• Willingness to travel as necessary (approximately 60%).

• Must reside in PA, NY, NJ, MA, ME, VT, NH, CT, or RI.

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Medical, dental, and vision insurance 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.

• Reasonable accommodations provided during the recruitment process.