Clinical Associate supporting the design, implementation, and management of clinical trials within a sponsor-dedicated model. The role involves coordinating study activities, maintaining documentation, and collaborating with cross-functional teams to ensure protocol adherence and regulatory compliance.
Responsibilities
Assist in planning, execution, and monitoring of clinical trials with protocol and regulatory adherence
Coordinate site initiation, patient recruitment, data collection, and monitoring visits
Collaborate with Clinical Operations, Data Management, and Biometrics teams on trial execution
Maintain comprehensive study documentation and records in compliance with regulations
Support study close-out activities including data cleaning and clinical report preparation




Requirements
Bachelor's degree in scientific or healthcare-related discipline
Previous clinical research or healthcare experience, preferably in pharmaceutical, biotechnology, or CRO sectors
Strong organizational and time management skills with ability to prioritize competing demands
Excellent attention to detail and problem-solving abilities focused on data accuracy and compliance
Effective communication and cross-functional collaboration skills
Willingness to travel approximately 60% as required
Legal right to work in Mexico

📌 Clinical Associate (Xico)
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