Clinical Research Associate

This is a fully remote position, open to applicants in Texas.

📋 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 the smooth execution of studies.

• Perform data evaluations and resolve queries to uphold high standards of clinical data quality.

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

• Assume responsibility for clinical trial monitoring deliverables while working collaboratively.

⛳️ Requirements

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

• A minimum of 2 years of experience as a Clinical Research Associate.

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

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

• Capacity to work both independently and collaboratively in a fast-paced setting.

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

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

🏝️ 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.