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 Role This 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 activities Operational involvement in study start-up and trial conduct Selective on-site monitoring, with a more balanced travel model Key Responsibilities Study Start-Up & Project Support Support 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 activities Support the preparation and maintenance of study plans, trackers, and project documentation Contribute to risk identification and mitigation activities during study conduct Trial Conduct & Management Support day-to-day trial execution activities, including site communication and issue follow-up Assist with oversight of timelines, deliverables, and study milestones Participate in cross-functional interactions with sponsors, vendors, and sites Contribute to the preparation of reports, status updates, and study documentation On-Site Monitoring Perform 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 requirements Review essential documents, source data, and data quality at site level Support sites in addressing findings and corrective actions] Profile We're Looking For Required Background 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 processes Willingness to travel for on-site monitoring Strong organizational skills and attention to detail Good communication skills in English (written and spoken) Desirable Experience supporting study start-up activities Exposure to project management or study coordination activities Experience working with international sponsors or CROs Why 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 scientificand 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