Study Start Up Associate I

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

📋 Description

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

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

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

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

• 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 offer insights on regulatory requirements and timelines.

⛳️ Requirements

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

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

• Exceptional attention to detail and strong organizational capabilities.

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

• Capacity to work independently and manage multiple tasks concurrently in a fast-paced environment.

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

• Legal authorization to work in Mexico.

🏝️ Benefits

• Competitive base salary and performance-related incentives.

• Health and wellbeing programs including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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