Clinical Research Associate

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

📋 Description

• Conduct site qualifications, initiate, monitor, and conclude visits for clinical trials.

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

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

• Review data 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.

⛳️ Requirements

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

• At least 2 years of experience as a Clinical Research Associate.

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

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

• Capacity to work both independently and as part of a team in a dynamic environment.

• Willingness to travel a minimum of 60% of the time (both internationally and domestically - by air and road).

• A valid driver’s license is required.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans available.

• Life insurance and disability coverage offered.

• Employee assistance programs and wellness resources provided.

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