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

📋 Description

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

• Ensure compliance with protocols, maintain data integrity, and prioritize patient safety throughout the trial process.

• Collaborate with investigators and site personnel to facilitate the smooth execution of studies.

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

• Contribute to the preparation and evaluation of study documentation, including protocols and clinical study reports.

• Take ownership of clinical trial monitoring deliverables and work in a collaborative manner.

⛳️ 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 processes, regulations, and ICH-GCP guidelines.

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

• Ability to function independently as well as collaboratively in a fast-paced environment.

• Willingness to travel as needed (approximately 40%).

• Legal authorization to work in Poland.

🏝️ 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 available.

• Life assurance and disability coverage provided.

• Employee assistance programs and wellness resources offered.

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