CTM II or Sr CTM (USA Scope) - Sponsor dedicated

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a CTM II or Sr CTM (USA Scope) - Sponsor dedicated in Brazil.

This role sits at the heart of clinical trial execution, ensuring high-quality delivery across complex, global studies with a strong focus on patient safety, regulatory compliance, and operational excellence. You will act as a key liaison between clinical sites, internal functional teams, and sponsors, overseeing study progress from site activation through closeout. Operating in a highly collaborative, international environment, you will combine strategic oversight with hands-on operational leadership. The position requires strong analytical thinking, risk-based decision-making, and the ability to coordinate multiple stakeholders across time zones. You will contribute directly to improving trial efficiency, data integrity, and patient outcomes in highly regulated clinical environments. This is a role for someone who thrives in complexity, autonomy, and cross-functional collaboration.

Accountabilities

In this position, you will be responsible for overseeing clinical trial site management activities, ensuring compliance with protocols, GCP, and regulatory requirements while safeguarding patient safety and data integrity. You will monitor study progress, identify risks, and implement mitigation strategies while coordinating across multiple functional teams and external stakeholders. The role also includes oversight of clinical monitoring deliverables, study documentation quality, and operational alignment across global trial activities.

• Oversee site management activities from activation through closeout, ensuring compliance and performance
• Monitor patient safety, protocol adherence, and data integrity across assigned studies
• Identify operational, quality, and timeline risks using clinical data, metrics, and dashboards
• Coordinate and align internal teams (CRA, Data Management, Patient Recruitment, etc.) to meet study milestones
• Act as escalation point for sites and support resolution of complex operational or compliance issues
• Review monitoring reports, study tools, and systems (CTMS, EDC, dashboards) for accuracy and completeness
• Support development and implementation of risk mitigation strategies and corrective action plans
• Ensure proper training, oversight, and performance management of CRAs and Central Monitors
• Participate in key study meetings, including kickoff and client-facing updates

Requirements

We are looking for a seasoned clinical research professional with strong experience in clinical trial management and site oversight within global or sponsor-dedicated environments. You should have deep knowledge of regulatory frameworks, risk-based monitoring, and operational trial execution. Strong leadership, communication, and problem-solving abilities are essential to succeed in this role.

• Bachelor’s degree or RN in a related field (or equivalent experience)
• Strong experience in clinical trial management, site monitoring, or central monitoring
• Proven ability to manage complex, global clinical studies and cross-functional teams
• Knowledge of ICH-GCP guidelines and regulatory compliance requirements
• Experience with risk-based monitoring methodologies is highly desirable
• Familiarity with clinical systems (CTMS, EDC, ePRO, dashboards, TMF)
• Strong analytical and problem-solving skills with a risk-management mindset
• Excellent communication, stakeholder management, and conflict resolution abilities
• Ability to work in international, matrixed environments
• Willingness to travel approximately 20%

Benefits

• Competitive global clinical research environment
• Fully remote work model based in Brazil
• Opportunity to work on large-scale, international clinical trials
• Exposure to sponsor-dedicated, high-impact studies
• Career development in a leading life sciences organization
• Collaborative and multicultural work environment
• Participation in complex, innovative drug development programs
• Learning and growth opportunities across global clinical operations

How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best!  Why Apply Through Jobgether?    Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.     #LI-CL1