Study Start Up Associate II

This is a fully remote position, open to applicants in Brazil, +1 more country.

📋 Description

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

• Support site start-up and activation efforts.

• Prepare and submit necessary regulatory documentation, such as clinical trial applications, ethics committee submissions, and communications with regulatory agencies.

• Coordinate and communicate with both internal and external stakeholders to secure approvals and authorizations for study initiation.

• Manage and keep precise records of regulatory submissions, approvals, and correspondence.

• Offer guidance and assistance to study teams regarding regulatory standards and best practices for study start-up.

• Engage in initiatives aimed at process improvement to optimize study start-up procedures and enhance overall efficiency.

⛳️ Requirements

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

• At least 2 years of experience in clinical research or regulatory affairs, specifically in study start-up activities.

• Strong familiarity with regulatory standards and guidelines for clinical trials, including ICH-GCP and local regulations.

• Outstanding organizational and project management abilities, with a capacity to prioritize and handle multiple tasks at once.

• Excellent communication and interpersonal skills, enabling effective collaboration with cross-functional teams.

• Willingness to travel as necessary (approximately 5%).

• 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.