Clinical Research Associate

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

📋 Description

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

• Ensure adherence to protocols, integrity of data, and safety of patients throughout the trial process.

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

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

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

• Operate within a sponsor-focused model, supporting the monitoring of cardiovascular and obesity trials.

⛳️ Requirements

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

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

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

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

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

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

• Must possess the legal right to work in the country where the position is located.

🏝️ 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 progression.