Jobs at Syneos Health

The Technical Customer Success Analyst assists teams in leveraging Syneos technology, provides support and training, manages communications, and tracks customer feedback and KPIs.

The Central Risk Manager is responsible for developing and implementing strategies for Risk-Based Quality Management and Monitoring across clinical trials, collaborating with stakeholders, and leveraging data analytics for risk identification and mitigation.

The Principal Site Grant Manager oversees investigator budget teams, resolves budgeting issues, develops budget templates, collaborates with stakeholders, and trains junior staff.

The role involves programming and data review for real-world data analysis, supporting epidemiologists, and managing complex data sets using statistical programming languages and tools.

Lead and independently negotiate US and Canadian clinical trial site Clinical Trial Agreements, amendments, and budgets. Manage contract lifecycle and tracking systems, coordinate execution and documentation, partner with cross-functional teams to drive study start-up, identify risks, mentor junior staff, and support process improvements and Sponsor stakeholder meetings.

Lead and oversee clinical development operations within Clinical Solutions, partnering with customers to deliver FSP or full-service trial execution, manage teams and resources, ensure operational excellence, and drive successful clinical trial delivery across drug development programs.

Lead or support real-world evidence studies by contributing to study design, conducting literature reviews and qualitative interviews, analyzing real-world data, preparing protocols, technical reports, manuscripts, and client presentations, and using statistical software and Microsoft Office to deliver timely, high-quality outputs for life sciences clients.

Lead and deliver operational and financial management of complex global clinical projects from proposal through closeout. Serve as primary client liaison, manage cross-functional teams, ensure GCP and regulatory compliance, maintain project tracking and inspection readiness, oversee budgets and deliverables, mentor/line-manage junior PMs, support business development, and implement risk mitigation and resource strategies. Travel ~25%.

Manage and coordinate clinical study deliverables, maintain TMF and inspection readiness, assist with interim analyses, vendor selection and management, financial reporting and budget reconciliation, facilitate team training, and support client communications and proposal activities to help meet study milestones.

Perform clinical review of oncology study participant-level data to ensure readiness for milestones (interim/final analyses, submissions). Conduct point-to-point and interpretive checks, generate and track queries, identify safety signals or protocol deviations, liaise with study teams, and follow SOPs to ensure data is clinically valid and submission-ready.

Lead development, negotiation, and management of US site budgets and clinical trial agreements. Negotiate with large academic institutions, draft templates, conduct due diligence (FMV, site justification), manage multiple contracting projects (oncology preferred), update trackers, ensure GCP and SOP compliance, train team members, and support process improvements to enable timely CTA execution.

Senior data analyst/programmer using SAS or R to analyze commercial claims and EHR real-world data. Create longitudinal cohorts, derive baseline/outcome variables, assess data quality, apply epidemiologic study designs and statistical methods (regression, survival), review protocols/SAPs, and program TFLs. Familiarity with OMOP CDM and OHDSI tools is a plus; prior pharmaceutical experience preferred.

The Project Financial Analyst II prepares and analyzes financial reports, facilitates client discussions, and provides financial insights to support business growth in the pharma/CRO sector.

Lead RWD analysis strategy and execution: develop technical specifications and statistical programs, perform complex observational analyses (propensity scoring, ML), validate cohorts/variables, ensure QC, collaborate cross-functionally, and communicate results to non-technical stakeholders.

The Clinical Scientist collaborates with Medical Directors to develop medical plans, reviews data for trends, manages project scopes, and ensures adherence to clinical protocols while participating in audits and meetings to improve study integrity.

The Clinical Scientist supports medical plan development, data analysis, and medical reviews while ensuring compliance with guidelines and project milestones.

The Clinical Scientist roles include developing medical plans, reviewing medical data, collaborating with study teams, and ensuring compliance with protocols and guidelines.

The Clinical Scientist in Oncology collaborates with Medical Directors to develop medical plans, perform data reviews, author queries, and manage project scope and quality, ensuring adherence to guidelines and timely project delivery.

Support Business Unit Controller with project accounting: record revenue, load budgets into Oracle/Revenue Wizard, produce monthly budget vs. actual variance analysis and forecasts, prepare reconciliations, review work/change orders, attend project meetings, monitor project health (revenue, gross profit, receivables, unbilled), and update financial reports and schedules.

Conduct site qualification, initiation, monitoring, management, and close-out visits to ensure protocol, regulatory and ICH/GCP compliance. Review source documents and CRFs, manage queries, investigational product handling, ISF/TMF reconciliation, documentation, and support audit readiness. Act as liaison with sites and sponsors, support recruitment/retention, and may train junior staff. Heavy travel (up to 75%).