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

📋 Description

• Perform site qualifications, initiations, monitoring, and close-out visits for clinical trials.

• Guarantee compliance with protocols, data integrity, and the safety of patients throughout the trial process.

• Work in partnership with investigators and site personnel to ensure efficient study execution.

• Conduct data reviews and address queries to uphold the quality of clinical data.

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

• Provide support for sponsor-specific monitoring of cardio and obesity-related trials.

⛳️ 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 procedures, regulations, and ICH-GCP guidelines.

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

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

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

• Legal eligibility 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 schemes.

• Life insurance and disability coverage.

• Employee assistance programs and resources for wellbeing.

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