Clinical Research Associate 2

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

📋 Description

• Participate in clinical trial monitoring activities, ensuring accountability for your deliverables while working collaboratively.

• Execute site qualification, initiation, monitoring, and close-out visits for clinical trials.

• Maintain protocol compliance, data integrity, and patient safety throughout the trial process.

• Work alongside investigators and site personnel to ensure smooth study execution.

• Conduct data reviews and resolve queries to uphold high-quality clinical data standards.

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

⛳️ Requirements

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

• Possess a minimum of 2 years of experience as a Clinical Research Associate.

• Have a thorough understanding of clinical trial processes, regulations, and ICH-GCP guidelines.

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

• Demonstrate the capability to work both independently and collaboratively in a fast-paced setting.

• Be willing to travel as needed (approximately 60%).

🏝️ Benefits

• Attractive 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 pathways.