Site Management Associate II

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

📋 Description

• Oversee monitoring activities at clinical trial sites, ensuring compliance with study protocols and prompt resolution of site-related issues.

• Support the preparation and review of regulatory documents, ensuring that site activities align with Good Clinical Practice (GCP) and relevant regulations.

• Work with cross-functional teams to enhance communication and provide support for trial sites throughout the entire study lifecycle.

• Monitor site performance metrics, analyze data, and generate reports to enhance the efficiency of site management.

• Engage in training programs and mentor junior staff to aid in their professional development in clinical trial management.

⛳️ Requirements

• A bachelor's degree in a relevant discipline such as life sciences, healthcare administration, or clinical research.

• Experience in clinical research, site management, or monitoring, with a comprehensive understanding of clinical trial processes and GCP guidelines.

• Strong organizational and project management abilities, capable of managing multiple priorities and meeting deadlines.

• Excellent analytical skills and meticulous attention to detail, committed to maintaining high-quality standards.

• Outstanding communication and interpersonal skills, with the capability to establish and sustain effective relationships with site personnel and cross-functional teams.

• Willingness to travel as needed (approximately 25%).

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.