Clinical Research Associate III

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

📋 Description

• Establish robust partnerships with clinical trial sites.

• Act as the main point of contact throughout the study execution.

• Oversee assigned sites throughout Phase One to Phase Four trials.

• Lead site initiation visits effectively.

• Carry out both remote and on-site monitoring activities.

• Proactively assess site performance and implement mitigation strategies.

• Foster early site engagement through feasibility assessments.

• Ensure comprehensive and precise study documentation.

• Assist in maintaining inspection readiness through audit preparation.

• Recognize opportunities for operational enhancements.

• Provide expertise on complex trials and mentor team members.

⛳️ Requirements

• Bachelor’s degree in a scientific, healthcare, or related discipline.

• A minimum of five years' experience in clinical research.

• In-depth knowledge of clinical trial processes as well as ICH and GCP guidelines.

• Familiarity with global regulatory expectations.

• Proven ability to independently manage multiple study sites.

• Strong analytical skills and risk-based decision-making capabilities.

• Willingness and capability to travel approximately fifty percent of the time.

🏝️ Benefits

• Health insurance.

• Retirement and wellbeing plans.

• Flexible working arrangements.

• Parental leave.

• Birthday day off.

• Employee recognition programs.

• Employee resource groups.

• Virtual self-development tools.