
Clinical Trial Manager, Project Management — Remote in Mexico
Syneos HealthClinical Trial Manager responsible for sponsor-dedicated monitoring, site oversight, project risk management, and clinical trial delivery at Syneos Health.


Clinical Trial Manager responsible for sponsor-dedicated monitoring, site oversight, project risk management, and clinical trial delivery at Syneos Health.

Support clinical research programs at Syneos Health by coordinating study timelines, budgets, vendors, recruitment, and cross-functional delivery. Help advance drug development through compliant clinical trial execution in Argentina.

Lead CMC submissions, lifecycle management, and global regulatory activities for Syneos Health’s life sciences services. Guide teams, clients, audits, and regulatory agency interactions.

Manage clinical monitoring and site activities for Syneos Health’s biopharmaceutical solutions business. Support regulatory compliance, data integrity, patient recruitment, and timely trial delivery.

Lead biomarker and genomics analyses using advanced statistics and deep learning to support clinical research and life sciences drug development at Syneos Health.

Lead clinical science activities for gynecologic oncology programs at Syneos Health, supporting medical data review, safety assessment, and eligibility decisions. Coordinate study teams, project deliverables, expert input, and medical review processes across integrated drug development projects.

Coordinate sponsor-site activities, regulatory documentation, clinical supplies, and study tracking for Syneos Health’s biopharmaceutical trials. Support site communications, meetings, audits, and corrective actions across assigned studies.

Senior Clinical Programmer responsible for SAS-based clinical programming, validation, and data management support at Syneos Health in Hyderabad. Leads programming delivery across three to ten concurrent studies and supports clinical teams, sponsors, audits, and technical operations.

Lead statistical programming for SDTM, ADaM, and TLF outputs at Syneos Health. Guide programming teams, validation, regulatory submissions, and CDISC compliance across life-sciences projects.

Lead site qualification, monitoring, compliance, and close-out activities for Syneos Health’s biopharmaceutical research programs in Mexico. Support data integrity, participant recruitment, audit readiness, and delivery against trial timelines.

Lead SAS-based programming for clinical trial outputs at Syneos Health, including datasets, tables, listings, and graphs. Coordinate validation, documentation, team leadership, and sponsor deliverables across multiple projects.

Lead clinical trial site management, monitoring, regulatory compliance, and risk oversight for Syneos Health’s research programs. Coordinate international study teams, systems, and trial deliverables from activation through closeout.

Support Syneos Health’s financial pricing systems and tools in a hybrid Belgrade role. The position covers pricing models, data maintenance, testing, troubleshooting, and tailored customer solutions.

Analyze project financial performance for Syneos Health’s life sciences services, covering reporting, budgets, forecasts, utilization, and profitability. Provide financial insights and clinical trial data analysis to support global management.

Lead SAS and CDISC programming for Syneos Health’s clinical-trial and regulatory submission work. Create validated datasets, statistical outputs, and programming standards across complex global studies.

Syneos Health is seeking a Mexico-based remote support associate to coordinate communications with patients, healthcare providers, and research sites. The role manages clinical research data, registries, and remote study activities.