Sr. Clinical Trial Manager. LATAM. Mexico. Argentina. Brazil. Chile.

Senior Clinical Trial Manager – LATAM Apply for the Senior Clinical Trial Manager role at Syneos Health in LATAM countries (Mexico, Argentina, Brazil, Chile). About Syneos Health Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model places the customer and the patient at the center of everything we do. We continuously seek ways to simplify and streamline our work, making Syneos Health easier to collaborate with and to work for. Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate about changing lives. Key Company Features We are passionate about developing our people through career development, progression, supportive line management, technical and therapeutic area training, peer recognition and total rewards. Our Total Self culture allows you to authentically be yourself. It unites us globally and focuses on caring for our people. We continuously build the company we all want to work for and our customers want to work with, fostering diversity of thought and belonging. Job Responsibilities Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. Oversees site interactions from activation through closeout, including patient recruitment, investigator payments and risk mitigations. Reviews study scope, budget and protocol, ensuring the clinical project team is aware of contractual obligations. Identifies risks to clinical trial management deliverables and escalates to the project manager. Employs strategic thinking and problem‑solving skills to propose and implement risk mitigations, and presents at key meetings such as Kick‑Off. Serves as escalation point for communications with investigator site staff, potentially interacting with principal investigators on the phone or in person. Collaborates with other functional leaders (Study Start‑Up, Patient Recruitment, Data Management) to coordinate delivery handoffs, meet milestones, and review functional plans. Develops and maintains clinical study tools and templates, including the Clinical Monitoring Plan. Ensures CTMS, dashboards and other systems are available, overseeing user acceptance testing. Coordinates training of the study team on protocol specifics, CRF completion, dashboards, SOPs, and timelines. Oversees resourcing allocations for CRAs and Central Monitors, site assignments, and identifies risks to delivery or quality. Reviews project oversight dashboards and other clinical trial systems (CTMS, EDC, eDiary, ePROs, TMF, IVRS/IWRS, dashboards) to monitor site activities, data updates, and compliance. Participates in development of the monitoring strategy and risk assessment plan; ensures team members understand, comply, and deliver according to monitoring strategy and risk plans. Reviews site and central monitoring documentation to ensure accurate representation of site management activities and risk communications. Provides status updates to clients, project management and leadership on deliverables and risks, offering solutions for protocol execution obstacles. Leads understanding of other functions’ roles (data management, study start‑up, patient recruitment, medical monitoring, pharmacovigilance, QA) to achieve compliance and delivery. Supports Inspection Readiness for clinical trial management scope. Oversees CRAs and Central Monitors, assesses training compliance, identifies emerging risks, and supports corrective action plans at site and study levels. Provides feedback to line managers on staff performance, strengths, and development areas. May be assigned to larger, more complex trials or coordinate clinical activities for a team of CTMs across a portfolio. May coach and mentor CTMs regarding functional delivery, risk evaluation, and action implementation. Moderate travel may be required, approximately 20%. Qualifications Bachelor’s degree or RN in a related field, or equivalent combination of education, training, and experience. Demonstrated ability to lead and align teams toward project milestones. Experience working in an international environment. Expertise in site management and monitoring (clinical or central). Preferred experience with risk‑based monitoring. Understanding of clinical trial management financial principles and budget management. Knowledge of Good Clinical Practice/ICH Guidelines and other regulatory requirements. Strong computer skills. Strong conflict‑resolution skills. Problem‑solving skills with risk‑management approach. Critical‑thinking skills for issue identification and solution determination. Moderate travel (~20%) may be required. Additional Information Tasks, duties, and responsibilities are not exhaustive. The Company may assign other tasks at its discretion. Equivalent experience or qualifications may be considered. The Company will determine what constitutes equivalent to the qualifications described. The statement does not create an employment contract. The Company complies with the Americans with Disabilities Act and provides reasonable accommodations as appropriate. Compliance & Equality The Company is committed to compliance with the Equality Directive and the Americans with Disabilities Act. All employment decisions are based on merit, qualifications, experience and competence, and not on gender, color, religion, national origin, disability, age, or sexual orientation. Summary Roles within the Clinical Trial Management job family are responsible for all aspects of the development, coordination, and implementation of Phase 1 clinical research studies. They collaborate with principal investigators, coordinate research subject interactions, and manage logistics and resources. They track study progress against project milestones, client deliverables, and budgets while ensuring compliance with global and regional regulations. Seniority Level Mid‑Senior level Employment Type Full‑time Job Function Research, Analyst, and Information Technology #J-18808-Ljbffr