Clinical Research Associate Ii (Chubut)

Clinical Research Associate II (FSP - Sponsor dedicated)

What You Will Do

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key 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.

Your Profile

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required Qualifications And Experience

• Ba...