Clinical Trial Manager (CTM)

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Clinical Trial Manager (CTM) based in Brazil. This is an opportunity to lead the operational delivery of clinical trials within a global research environment. You will oversee study execution across timelines, quality standards, budgets, protocols, and regulatory requirements. The role involves close collaboration with CROs, vendors, clinical sites, and multidisciplinary research teams. You will serve as a key point of coordination between international teams and US-based pharmaceutical stakeholders. Your expertise will help identify risks, resolve operational challenges, and keep studies progressing effectively. The position offers significant responsibility in a remote, international setting supporting pharmaceutical research. It is well suited to an experienced clinical research professional who combines strong project management with scientific rigor and communication skills. Lead the day-to-day operational execution and oversight of assigned clinical trials, ensuring activities remain aligned with protocols, timelines, quality standards, budgets, and applicable regulations. Develop and maintain study timelines, milestones, operational plans, and key deliverables. Coordinate CROs, vendors, clinical sites, and external partners, ensuring effective collaboration and timely execution. Monitor study progress, identify risks, issues, and potential delays, and implement appropriate mitigation strategies. Ensure trial activities comply with ICH-GCP, applicable regulatory requirements, protocols, and established SOPs. Collaborate with Clinical Operations, Regulatory, Medical, Data Management, Pharmacovigilance, Biostatistics, and other cross-functional teams. Track study metrics, KPIs, quality indicators, and operational deliverables, following up on actions where needed. Support study budgets, vendor management, financial tracking, and related operational activities. Prepare and participate in study team meetings and presentations for internal and external stakeholders. Communicate study status, risks, milestones, and key decisions clearly to US-based stakeholders. Requirements: Bachelor's degree in Life Sciences, Pharmacy, Nursing, Medicine, or a related discipline. At least 3 years of professional experience in clinical research, including relevant experience in Clinical Trial Management or Clinical Operations. Experience managing clinical trials within a pharmaceutical, biotechnology, CRO, or related healthcare organization. Solid knowledge of ICH-GCP, clinical research processes, and applicable regulatory requirements. Experience coordinating CROs, vendors, clinical sites, and cross-functional teams. Strong project management, organizational, analytical, and problem-solving capabilities. Ability to manage multiple priorities, risks, and deadlines effectively in a remote and international environment. Excellent written and verbal communication skills, with the confidence to work directly with US-based stakeholders. Advanced English proficiency at C1 level or equivalent. Strong proficiency with Microsoft Office and commonly used clinical trial or project management systems. Experience with global or multinational clinical trials is preferred. Previous collaboration with US-based pharmaceutical clients or stakeholders is advantageous. Experience in Phase I–III clinical development and electronic clinical trial systems is a plus. PMP, ACRP, SOCRA, or another relevant clinical research/project management certification is desirable. Benefits: Competitive salary paid in USD . 100% remote work from Latin America. Long-term professional engagement. Independent Contractor arrangement. 10 business days / 2 weeks of paid time off . Paid US-calendar holidays . Full-time working schedule aligned with EST hours. Opportunity to collaborate with international clinical research teams and US-based pharmaceutical stak