Clinical Research Associate

This is a fully remote position, open to applicants in Florida, +3 more states.

📋 Description

• Design and evaluate clinical trials while interpreting intricate medical data.

• Participate in clinical trial monitoring activities and assume responsibility for deliverables.

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

• Ensure adherence to protocols, data integrity, and patient safety.

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

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

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

⛳️ Requirements

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

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

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

• Experience in monitoring Ophthalmology trials or multi-therapeutic areas.

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

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

• Willingness to travel as necessary, approximately 60% of the time.

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

🏝️ Benefits

• Competitive base salary.

• Performance-related incentives.

• Medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Learning and development opportunities through structured training and career pathways.