Descripción del trabajoLead requirement gathering sessions and translate business needs into clear, actionable technical documentationSupport end-to-end clinical trial management processes—from study initiation to closeout—including internal and FDA reportingEnsure compliance with industry standards such as GCP, Good Documentation Practices, and Clinical Trial Quality guidelinesCollaborate with cross-functional teams in an Agile environment to deliver scalable, high-quality solutionsPerform business analysis and use case modeling to support system design and developmentParticipate in the full Software Development Life Cycle (SDLC), preferably within pharma IT platforms Required Skills and ExperienceBachelor’s degree in a relevant field or equivalent experience5+ years of experience in IT, with a focus on clinical systems and healthcare technologyStrong understanding of clinical trial workflows and regulatory requirementsExcellent communication and stakeholder engagement skillsHands-on experience with Agile methodologies and business analysis practicesMust be authorized to work in the U.S. without employer-based visa sponsorship Nice to Have SkillsExperience in consulting environments with flexibility to travelStrong planning, coordination, and analytical capabilities