Clinical Research Associate – Sponsor Dedicated

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

📋 Description

• Participate in clinical trial monitoring activities, taking ownership of deliverables and collaborating effectively.

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

• Ensure adherence to protocols, data integrity, and patient safety throughout the trial process.

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

• Review data and resolve queries to uphold the quality of clinical data.

• Assist 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 field.

• A minimum of 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 keen eye for detail.

• Capability to work both independently and as part of a team in a fast-paced environment.

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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