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

📋 Description

• Oversee the commencement of clinical trials, ensuring adherence to regulatory standards.

• Execute site start-up and activation tasks to a high-quality standard.

• Aid in the preparation and submission of regulatory documents, encompassing clinical trial applications and ethics committee submissions.

• Collaborate with both internal and external stakeholders to secure approvals and authorizations for the initiation of studies.

• Keep precise and current records of regulatory submissions and approvals.

• Assist study teams in crafting protocols, informed consent documents, and investigator brochures.

• Engage in study start-up meetings, contributing insights on regulatory requirements and timelines.

⛳️ Requirements

• Bachelor's degree in life sciences or a similar field.

• Previous experience in clinical research or regulatory affairs is preferred but not mandatory.

• Experience in study start-up or site activation within Brazil.

• Exceptional attention to detail and strong organizational skills.

• Outstanding communication and interpersonal abilities, with a knack for effective collaboration across cross-functional teams.

• Capacity to work independently while managing multiple tasks concurrently in a dynamic environment.

• 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.