Site Management Associate

This is a fully remote position, open to applicants in Brazil, +2 more states.

📋 Description

• Assist in overseeing clinical trial sites.

• Ensure compliance with study protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.

• Provide support for site management tasks, which include preparing documentation, entering data, and monitoring site performance metrics.

• Work collaboratively with cross-functional teams to enhance communication and resolve site-related challenges.

• Keep precise records of site activities.

• Aid in the development of monitoring reports.

• Engage in training and development programs to improve knowledge and skills in clinical trial management.

⛳️ Requirements

• Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.

• Experience in supporting global clinical research, site management, or similar administrative positions.

• Exceptional organizational abilities and meticulous attention to detail.

• Capability to efficiently manage multiple tasks.

• In-depth knowledge of clinical trial processes and regulatory requirements.

• Strong communication and interpersonal skills.

• Ability to work effectively in a collaborative global team environment.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary.

• Performance-related incentives.

• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

• Learning and development opportunities through structured training and career pathways.