
10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
🔥 2 minutes ago
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10,000+ employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
• Provide site management oversight, clinical monitoring and central monitoring deliverables, focusing on patient safety, protocol/GCP/regulatory compliance and data integrity • Oversee site interactions from activation through closeout, including recruitment, investigator payments and related activities • Identify critical data, process and protocol-execution risks and develop mitigations using the RACT • Review study scope, budget and protocol content and ensure clinical project teams understand contractual obligations • Identify and escalate risks to timelines, quality, budget and contracted scope • Participate in and present at key meetings, including Kick Off Meetings • Serve as an escalation point for investigator site staff communications and interact with investigators and site staff by phone or in person • Collaborate with Study Start Up, Patient Recruitment, Data Management and other functions to meet study milestones • Develop and maintain clinical study tools and templates, including Clinical Monitoring Plans • Ensure CTMS, dashboards and other systems are configured and available, including user acceptance testing and access/audit trail reviews • Coordinate study-team training on protocols, CRF completion, dashboards, SOPs, clinical plans, data plans and timelines • Oversee CRA and Central Monitor resourcing, site assignments and study-team conduct • Ensure quality and visibility of clinical monitoring, central monitoring and site management deliverables • Review oversight dashboards and clinical trial systems including CTMS, EDC, eDiary, ePRO, TMF, IVRS/IWRS and central monitoring dashboards • Oversee compliance with monitoring strategies, CMP/SMP and risk plans • Review site and central monitoring documentation and ensure timely, compliant delivery • Provide client, project management and leadership updates on deliverables and risks • Support inspection readiness, corrective action plans, data cuts and database lock deadlines • Oversee CRAs and Central Monitors, assess compliance and identify emerging risks • Provide staff-performance feedback to line managers; may support larger, more complex trials
• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience • Demonstrated ability to lead and align teams in the achievement of project milestones • Demonstrated capability of working in an international environment • Demonstrated 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 applicable regulatory requirements • Good computer skills • Good communication, presentation and interpersonal skills among project team and with sites • Strong conflict resolution skills • Ability to apply problem-solving techniques to resolve complex issues and apply a risk management approach • Critical thinking to determine causes and appropriate solutions to issues • Moderate travel may be required, approximately 20%
• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Total Self culture supporting authenticity and inclusion • Diversity, equity and belonging initiatives
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🇲🇽 Mexico – Remote
💰 $75M Private Equity Round on 2015-12
⏰ Full Time
🟠 Senior
🔴 Lead
🧪 Clinical Research