CTM II – Sr CTM assigned to client LAtam (USA scope)

About This Opportunity

Our talent team is representing a confidential biopharmaceutical services organization seeking a Senior Clinical Trial Manager for their Latin America region. This remote position supports clinical development projects with a focus on site management, monitoring oversight, and compliance across Argentina, Brazil, Chile, Colombia, and Mexico, with USA-scope protocol responsibilities.

The role is ideal for an experienced clinical professional who has led site teams, managed monitoring strategies, and ensured protocol execution across international markets.

Responsibilities

• Oversee site management from activation through closeout, including patient recruitment coordination and investigator payments
• Lead clinical monitoring and central monitoring deliverables with focus on patient safety, GCP compliance, and data integrity
• Develop and maintain clinical study tools including the Clinical Monitoring Plan and ensure proper CTMS and dashboard setup
• Review protocol scope, budget, and contractual obligations; escalate risks to timelines, quality, or budget to project management
• Serve as escalation point for investigator site communications and may accompany CRAs for site observation or conflict resolution
• Coordinate with Study Start Up, Patient Recruitment, and Data Management teams to meet enrollment targets and database lock timelines
• Provide initial and ongoing training to study teams on protocol requirements, CRF completion, SOPs, and data plans
• Oversee resourcing allocations for CRAs and Central Monitors, including site assignments and performance quality
• Review monitoring documentation (visit reports, site letters, central monitoring reports) to ensure quality standards and timely delivery
• Monitor project dashboards and clinical trial systems (CTMS, EDC, ePRO, TMF, IVRS/IWRS) to track site and patient activities
• Support inspection readiness activities and corrective action plans at site and study level
• Participate in and present at key meetings such as Kick Off Meetings
• Provide status updates and solutions to clients and leadership regarding clinical deliverables and protocol execution obstacles

What We're Looking For

• Bachelor's degree or RN in a related field, or equivalent combination of education, training, and experience
• Demonstrated expertise in site management and clinical or central monitoring
• Proven ability to lead and align teams in achieving project milestones in an international environment
• Experience with risk-based monitoring strategies preferred
• Understanding of clinical trial financial principles and budget management
• Strong knowledge of Good Clinical Practice/ICH Guidelines and applicable regulatory requirements
• Excellent communication, presentation, and interpersonal skills for interactions with project teams and sites
• Strong conflict resolution and problem-solving skills with ability to apply risk management approaches
• Critical thinking capability to identify root causes and develop appropriate solutions for complex issues
• Proficiency with computer systems and clinical trial technology platforms
• Willingness to travel approximately 20% as needed
• Fluency in English required; Spanish or Portuguese strongly preferred for Latin America scope

How We Work With You

When you apply through Get A Job.ai, one of our specialized recruiters will review your background and conduct an initial screening. If there's a strong match, we'll prepare and submit your profile to our client for consideration. Please do not contact the employer directly—all communication and interview coordination will be managed through our team to ensure the best experience for you and our client.

Pay

Compensation details will be discussed during the screening process and are based on experience and qualifications.

Equal Opportunity: Get A Job.ai is committed to inclusive hiring practices. We welcome applications from candidates of all backgrounds and provide equal employment opportunities regardless of race, color, religion, gender, national origin, age, disability, or veteran status.