Jobs at Syneos Health

Lead statistical activities for early-phase clinical studies from protocol through CSR: prepare SAPs, generate randomization, oversee SAS programming and QC, interact with sponsors and regulators, mentor biostatistics staff, and ensure timelines and inspection readiness.

The Director of Epidemiology Pipeline collaborates on virology clinical trials, providing scientific expertise, leading project proposals, and overseeing study management and regulatory compliance.

Prepare, reconcile, analyze and report business unit revenue, contracts, projects and related metrics. Load and maintain project budgets and data in Oracle/Revenue Wizard, draft monthly actual vs. budget/forecast analyses, support forecasting and backlog submissions, perform project close-outs and reconciliations, attend project meetings, and monitor project financial health (revenue, gross profit, receivables, unbilled amounts).

The Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.

Perform site qualification, initiation, monitoring, management and close-out visits (on-site or remote) ensuring ICH-GCP and protocol compliance. Verify informed consent, source documents, CRF accuracy, IP handling, ISF/TMF reconciliation, and EDC compliance. Document findings, support query resolution, site training, audit readiness, and collaborate with project teams, sponsors and local staff. May perform chart abstraction and real-world late phase site support.

Lead statistical programmer responsible for developing SAS (and R) code to produce tables, listings, and figures per SAP; direct and mentor programming staff; ensure data integrity; troubleshoot issues; collaborate with statisticians; and improve programming processes during a 1.5-year assignment.

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 execute statistical programming activities including migration to SAS Viya, development of tables/listings/figures and derived datasets, CDISC compliance (SDTM/ADaM/DEFINE.XML), process improvement, mentoring, quality control, regulatory submission readiness, client interfacing, and contributing to SOPs and business development. Ensures documentation, inspection readiness, and adherence to industry standards.

Manage a multifunctional clinical operations/data review team in an FSP environment, ensuring quality deliverables, KPI compliance, customer issue escalation, resource planning, revenue impact, and people leadership including performance management, training, workload oversight, and staff development.

The CRA II/Senior CRA will perform site management activities, ensure compliance with regulations, conduct monitoring visits, and support recruitment efforts throughout the clinical trial process.

The Manager of Biostatistics oversees biostatisticians, ensuring project quality, adherence to regulations, and managing staff development while meeting financial targets.

The Principal Biostatistician oversees statistical tasks, mentors staff, prepares analyses, and ensures high-quality deliverables throughout project lifecycle.

The Principal Statistician oversees biostatistics projects, mentors staff, prepares statistical plans, and ensures quality and regulatory compliance in clinical trials.

Oversee biostatistical activities, mentor staff, prepare statistical plans, ensure quality control, and manage multiple clinical projects while interfacing with regulatory agencies.

Lead statistical programming for clinical trials using SAS to produce SDTM and ADaM datasets, tables, listings, and figures. Ensure quality and regulatory compliance (CDISC, DEFINE.XML), validate outputs, manage schedules, mentor programmers, participate in sponsor meetings, and serve as a technical SME for standards and submissions.

The Executive Assistant provides high-level administrative support to the Business Unit Head, managing calendars, travel, communications, and preparing executive presentations. Skills needed include organization, discretion, and strong communication.

Ensure effective clinical research operations, monitor study progress, adhere to regulations, and coordinate communication with clinical trial participants.

The Principal Biostatistician leads biomarker-related statistical activities in clinical studies, develops evaluation plans, and performs complex data analysis, focusing on genomics and biomarkers.

Lead sponsor-dedicated epidemiology and real-world evidence (RWE) scientific strategy across multiple European countries. Provide scientific oversight for study design and execution, develop proposals and study documents (protocols, SAPs, reports), support business development, ensure regulatory and methodological compliance, build organizational RWE capabilities and SOPs, and produce scientific communications (abstracts, manuscripts, presentations).

Lead digital recruitment strategies for clinical trials. Provide strategic counsel to sponsors, oversee digital recruitment channels, and track performance using data insights.