Study Start Up Associate I

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

📋 Description

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

• Deliver high-quality site start-up and activation tasks.

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

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

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

• Aid study teams in the development of protocols, informed consent forms, and investigator brochures.

• Engage in study start-up meetings and contribute 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.

• Exceptional attention to detail and strong organizational abilities.

• Outstanding communication and interpersonal skills, with the capacity to collaborate effectively across cross-functional teams.

• Capability to work independently and juggle multiple tasks in a fast-paced environment.

• Advanced proficiency in English is essential.

• 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 assurance and disability coverage.

• Employee assistance programs and wellness resources.

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