Clinical Research Associate

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

📋 Description

• Conduct site qualifications, initiate, monitor, and perform 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.

• 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.

• Operate within a sponsor-dedicated model focused on supporting cardiovascular and obesity trials.

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

⛳️ Requirements

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

• A minimum of 2 years of experience in the role of a Clinical Research Associate.

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

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

• Capacity to work independently and collaboratively in a dynamic environment.

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

• Legal authorization 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 available.

• Life insurance and disability coverage provided.

• Employee assistance programs and wellness resources accessible.

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