Clinical Study Team Assistant – Patient Recruitment

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

📋 Description

• Assist in overseeing clinical trial sites.

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

• Support activities related to site management, including documentation preparation, data entry, 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 creation of monitoring reports.

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

⛳️ Requirements

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

• Preferred but not mandatory: some experience in clinical research, site management, or similar administrative roles.

• Strong organizational abilities and attention to detail, with the capacity to efficiently manage multiple tasks.

• Basic understanding of clinical trial processes and regulatory requirements is advantageous.

• Outstanding communication and interpersonal abilities, with a knack for working collaboratively in a team setting.

• 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, which may include medical, dental, and vision coverage.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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