Clinical Research Associate

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

📋 Description

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

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

• Collaborate with investigators and site personnel to ensure the efficient conduct of studies.

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

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

• Design and analyze clinical trials, interpret complex medical data, and contribute to the development of innovative treatments and therapies.

• Assume responsibility for deliverables and work effectively within a sponsor-dedicated framework.

⛳️ Requirements

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

• At least 1 year of experience as a Clinical Research Associate.

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

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

• Capability 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 role 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 wellbeing resources.

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

• Reasonable accommodations provided during the recruitment process.