Senior Clinical Research Associate

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

📋 Description

• Establish and manage a study

• Finalize study status reports

• Organize and maintain study documentation

• Engage in the submission of protocols and consent forms for ethics/IRB approval

• Aid in the preparation of regulatory submissions as necessary

⛳️ Requirements

• Bachelor’s degree in a life science or a related field

• At least 5 years of experience in independent site monitoring

• Minimum of 2 years in the oncology field

• Knowledge of ICH GCP Compliance

• Exceptional time management and interpersonal skills

• Highly driven with an excellent attention to detail

• Willingness to travel domestically and internationally for approximately 65%-75% of work time

• Valid driver’s license is required

🏝️ Benefits

• Competitive salary

• Comprehensive benefits package

• Medical care plan: Health, Dental & Vision

• Life Assurance

• Supportive work environment

• Emphasis on teamwork and collaboration

• Outstanding training opportunities