Site Management Associate II

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

📋 Description

• Assist in the management and oversight of clinical trial sites.

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

• Coordinate monitoring activities across clinical trial sites.

• Guarantee compliance with study protocols and prompt resolution of site-related challenges.

• Aid in the preparation and review of regulatory documents.

• Collaborate with cross-functional teams throughout the entire study lifecycle.

• Monitor site performance metrics, analyze data, and generate reports.

• Engage in training programs and mentor junior team members.

⛳️ Requirements

• A Bachelor's degree in a relevant area 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, focused on upholding high-quality standards.

• Outstanding communication and interpersonal skills, adept at establishing and maintaining effective relationships with site personnel and cross-functional teams.

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

• Legal authorization to work in Brazil.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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