Clinical Research Associate III

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

📋 Description

• Establish robust collaborations with clinical trial sites.

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

• Facilitate site initiation visits and ensure that site teams receive comprehensive training.

• Perform both remote and on-site monitoring activities.

• Assess site performance proactively and execute mitigation strategies.

• Foster early site engagement through feasibility assessments.

• Ensure all study documentation is complete and accurate.

• Assist in maintaining inspection readiness through audit preparations.

• Recognize opportunities for operational enhancements and collaborate with sites.

⛳️ Requirements

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

• Minimum of five years’ experience in clinical research.

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

• Knowledge of global regulatory expectations.

• Proven ability to independently manage multiple study sites.

• Excellent communication and stakeholder management skills.

• Strong analytical skills and the capability for risk-based decision-making.

• Willingness to travel approximately fifty percent of the time.

🏝️ Benefits

• Competitive salary.

• Annual bonus.

• Life insurance.

• Retirement and wellbeing plans.

• Health insurance.

• Flexible working arrangements.

• Parental leave.

• Birthday day off.

• Employee recognition programs.

• Employee resource groups.

• Virtual self-development tools.