Site Activation Partner I

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

📋 Description

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

• Execute site start-up and activation tasks to an exemplary level.

• Draft and submit regulatory paperwork, including clinical trial applications and ethics committee submissions.

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

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

• Assist study teams in creating essential study documents, such as protocols, informed consent forms, and investigator brochures.

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

⛳️ Requirements

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

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

• Familiarity with local Ethics Committee requirements and submission protocols is essential.

• Exceptional attention to detail and strong organizational capabilities.

• Outstanding communication and interpersonal skills, with the capacity to work collaboratively with cross-functional teams.

• Ability to work autonomously and manage multiple tasks concurrently in a dynamic environment.

• Legal authorization to work in the country where this 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 advancement pathways.