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

📋 Description

• Execute site qualifications, initiation, monitoring, and closure visits for clinical trials.

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

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

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

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

• Assume responsibility for clinical trial monitoring deliverables and collaborate effectively within a sponsor-dedicated framework.

⛳️ Requirements

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

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

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

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

• Legal eligibility to work in Bulgaria.

🏝️ 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 pathways.