CRA I, CRA II, Senior CRA

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

📋 Description

• Execute clinical trial monitoring tasks to a superior standard

• Oversee all processes involved in establishing and monitoring a study

• Produce precise study status reports and uphold study documentation

• Address sponsor-generated queries effectively

• Assume responsibility for the cost efficiency of the study

• Engage in the preparation and assessment of study documentation and feasibility studies for new proposals

• Build and sustain cooperative relationships with key stakeholders, clinical investigators, and site personnel

• Ensure patient safety and adherence to ICON's procedures, protocols, and regulatory standards

⛳️ Requirements

• Bachelor's degree in medicine, science, or an equivalent field

• Relevant experience in clinical trial monitoring

• Familiarity with ICH-GCP guidelines

• Ability to review and assess medical data

• Exceptional written and verbal communication skills in English

• Strong interpersonal skills to handle queries promptly

• Openness to travel as necessary (approximately 60%)

• Legal authorization to work in the country where the position is located

🏝️ Benefits

• Attractive 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