Senior Clinical Data Associate role at Thermo Fisher Scientific supporting clinical trial data management across multiple studies. Responsible for data quality, integrity, and compliance while collaborating with cross-functional teams on study delivery in a hybrid environment based in Mexico City.
Responsibilities
Review, clean, and reconcile clinical data to ensure accuracy, completeness, and regulatory compliance across studies
Generate and resolve data queries while maintaining clinical database integrity and quality standards
Independently manage data management deliverables and timelines across multiple concurrent studies
Mentor junior team members and provide technical guidance on study-specific data management processes
Collaborate with Clinical Operations, Biostatistics, and cross-functional teams to support study execution
Requirements




Bachelor's degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or related scientific field
Minimum 3–5 years of Clinical Data Management experience in pharmaceutical, biotechnology, CRO, or medical device industry
Demonstrated experience managing multiple clinical studies simultaneously
Proficiency with Electronic Data Capture systems such as Medidata Rave, Inform, Veeva CDMS, or Oracle InForm
Strong knowledge of Good Clinical Practice, ICH guidelines, and Clinical Data Management principles
Excellent analytical, critical thinking, and problem-solving skills with exceptional attention to detail

📌 Sr Clin Data Assoc (Xico)
🏢 Thermo Fisher Scientific
📍 Xico