Clinical Research Associate II

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

📋 Description

• Participating in monitoring activities for clinical trials, taking charge of deliverables and collaborating effectively.

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

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

• Working alongside investigators and site personnel to ensure the smooth execution of studies.

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

• Assisting in the preparation and evaluation of study documentation, which includes 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.

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

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

• 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 where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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