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

📋 Description

• Oversee the initiation of clinical trials while ensuring adherence to regulatory standards.

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

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

• Collaborate with both internal and external stakeholders to secure approvals and authorizations for study commencement.

• Ensure accurate and current records of regulatory submissions and approvals are maintained.

• Assist study teams in the creation of study documents, such as protocols, informed consent forms, and investigator brochures.

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

⛳️ Requirements

• A Bachelor's degree in life sciences or a related discipline.

• Prior experience in clinical research or regulatory affairs is preferred, though not mandatory.

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

• Exceptional attention to detail along with strong organizational abilities.

• Outstanding communication and interpersonal skills, with a capability to work effectively in cross-functional teams.

• Capacity to work independently while managing multiple tasks simultaneously 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 schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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