Clinical Development Analyst

Location: Brazil (hybrid / remote with on-site visits)Type: 12-month contract (high possibility of further renewals)Clinergy Health is a boutique CRO focused on delivering high-quality, highly tailored clinical development solutions for pharmaceutical and biotech companies operating in Brazil and Latin America. We deliberately work with a selected number strategic projects ranging from phase 1 to RWE to ensure scientific rigor, operational excellence, and close collaboration with our clients.We are now expanding our team and looking for a Clinical Trials Analyst to support our growing portfolio of clinical development projects.The RoleThis position is ideal for a professional with previous experience in clinical trial monitoring who is looking to expand beyond a traditional CRA role looking into further professional development.As a Clinical Trials Analyst, you will work closely with the Project Lead, supporting key activities across the entire study lifecycle — from start-up through execution — while maintaining hands-on involvement in on-site monitoring.This is a hybrid role, combining:Strategic and analytical project-support activitiesOperational involvement in study start-up and trial conductSelective on-site monitoring, with a more balanced travel modelKey ResponsibilitiesStudy Start-Up & Project SupportSupport clinical trial start-up activities (site selection, feasibility support, essential documents, regulatory and ethics submissions follow-up)Assist the Project Lead in planning, tracking, and coordinating study activitiesSupport the preparation and maintenance of study plans, trackers, and project documentationContribute to risk identification and mitigation activities during study conductTrial Conduct & ManagementSupport day-to-day trial execution activities, including site communication and issue follow-upAssist with oversight of timelines, deliverables, and study milestonesParticipate in cross-functional interactions with sponsors, vendors, and sitesContribute to the preparation of reports, status updates, and study documentationOn-Site MonitoringPerform on-site monitoring visits according to the monitoring plan (e.g., initiation, routine, and close-out visits)Ensure compliance with protocol, GCP, and applicable regulatory requirementsReview essential documents, source data, and data quality at site levelSupport sites in addressing findings and corrective actions]Profile We're Looking ForRequiredBackground in Life Sciences (e.g., Pharmacy, Biology, Biomedicine, Nursing, or related fields)Previous experience in clinical trials monitoring (CRA or similar role)Solid understanding of GCP and clinical trial processesWillingness to travel for on-site monitoring Strong organizational skills and attention to detailGood communication skills in English (written and spoken)DesirableExperience supporting study start-up activitiesExposure to project management or study coordination activitiesExperience working with international sponsors or CROsWhy Join Clinergy Health?Broader role than a traditional CRA position, with exposure to strategic and project-level activities;Real development opportunity in clinical trial management and oversight;Balanced travel model, avoiding the heavy travel burden typical of monitoring-only roles;Close collaboration with highly experienced clinical development professionals;High scientific and regulatory standards, with real ownership of your work;Highly competitive compensation rates.Note: this role will initially be a 12-month contract position with the possibility of further renewals and/or beaconing a permanente role.If you are looking to grow beyond monitoring, gain a deeper understanding of how clinical trials are planned and managed, and work in a focused, high-quality CRO environment, we would be happy to hear from you.Applications: online via LinkedIn advertisement or by sending your resume to info@clinergyhealth.com