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

📋 Description

• Performing site qualification, initiation, monitoring, and closure visits for clinical trials.

• Ensuring adherence to protocols, maintaining data integrity, and prioritizing patient safety throughout the trial.

• Collaborating with investigators and site personnel to ensure effective study execution.

• Conducting data reviews and resolving queries to uphold the quality of clinical data.

• Assisting in the preparation and evaluation 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.

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

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

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage when 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 pathways.