Study Start Up Associate I

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

📋 Description

• Facilitate the commencement of clinical trials while ensuring adherence to regulatory standards.

• Execute site start-up and activation tasks to a high level of excellence.

• Aid in the preparation and submission of regulatory documentation, such as clinical trial applications and ethics committee submissions.

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

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

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

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

⛳️ Requirements

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

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

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

• Exceptional attention to detail and strong organizational abilities.

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

• Capability to work independently and manage various 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 schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Learning and development opportunities through structured training and career pathways.