Clinical Research Associate

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

📋 Description

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

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

• Collaborate with investigators and site staff to ensure the smooth execution of studies.

• Perform data review and address queries to uphold high-quality clinical data.

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

• Take ownership of deliverables and work collaboratively on clinical trial monitoring activities.

⛳️ Requirements

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

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

• Experience in monitoring hem/onc studies.

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

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

• Capability to work independently and in a team-oriented, fast-paced 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-based incentives.

• Medical, dental, and vision coverage as 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.