Clinical Research Associate II — Global Trials & Data

ICON Clinical Research; Santiago; Remote; CLP 18,000,000 - 24,000,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance programme (LifeWor

Life insurance

Childcare vouchers

Job summary

ICON Strategic Solutions in Chile seeks a CRA II to design and analyse clinical trials, interpreting data and contributing to innovative therapies. You will conduct site qualification, initiation, monitoring and close-out visits, ensuring protocol compliance and patient safety.

Requirements: a Bachelor's degree in a scientific field, at least 2 years as a Clinical Research Associate, knowledge of ICH-GCP, strong organization and communication skills, and willingness to travel ~60%.

Qualifications

• Bachelor's degree in a scientific field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required (approximately 60%).

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Skills

Clinical monitoring

ICH-GCP knowledge

Data integrity

Communication skills

Education

Bachelor's degree in a scientific field

Job description

ICON Strategic Solutions in Chile seeks a CRA II to design and analyse clinical trials, interpreting data and contributing to innovative therapies. You will conduct site qualification, initiation, monitoring and close-out visits, ensuring protocol compliance and patient safety.

Requirements: a Bachelor's degree in a scientific field, at least 2 years as a Clinical Research Associate, knowledge of ICH-GCP, strong organization and communication skills, and willingness to travel ~60%.