Clinical Operations Associate

This is a fully remote position, open to applicants in Brazil, +2 more countries.

📋 Description

• Assist clinical study teams with administrative and operational responsibilities.

• Oversee site payments and the supply chain for clinical trials.

• Organize and maintain critical study documentation within electronic systems.

• Execute activities related to the Trial Master File (TMF) to ensure readiness for inspections.

• Monitor, gather, scan, file, and manage study documents and Case Report Forms (CRFs).

• Offer limited site-facing assistance in collaboration with Clinical Research Associates.

• Collaborate closely with Clinical Research Associates and project teams throughout the clinical trial process.

⛳️ Requirements

• Prior experience at a clinical research site (Site Coordinator, Research Coordinator, or similar positions).

• Proficient in English is mandatory.

• Competent in Microsoft Office applications.

• Capable of juggling multiple priorities in a dynamic environment.

• Excellent organizational abilities and meticulous attention to detail.

• A university degree in healthcare, life sciences, or a related discipline.

🏝️ Benefits

• Opportunities for continuous learning and professional development.

• Flexible work arrangements.

• Promotes a healthy work-life balance.

• Be part of a collaborative, diverse, and supportive global team.

• Gain exposure to a wide array of clinical operations activities and career pathways.