Jobs at Syneos Health

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.

Lead and deliver statistical activities across clinical trial lifecycle: prepare SAPs, generate randomization schedules, review CRFs and database design, coordinate biostatistics and programming teams, perform QC/verification, support regulatory interactions, mentor staff, and contribute to business development. Minimal travel.

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.

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.

Provides subject matter expertise in clinical trial risk-based and centralized monitoring strategies. Develops risk assessments, supports RACT finalization, identifies and tracks study risks, advises on mitigation plans, evaluates remote data review tools, facilitates risk findings with cross-functional teams and sponsors, supports Quality Tolerance Limits, delivers training, ensures compliance and inspection readiness, and contributes to monitoring strategy budgets and proposals.

Performs clinical data management activities for Phase I–III trials, including ongoing data review, reconciliation of third-party and serious adverse event data, user acceptance testing and quality control of clinical databases, and maintenance of data management documentation in accordance with ICH/GCP requirements.

Conduct real-world data analyses using SAS or R and commercial claims and EHR databases. Build longitudinal study cohorts, define baseline and outcome variables, apply epidemiologic methods, perform statistical tests, regression and survival analyses, assess data quality, review protocols and statistical analysis plans, and program tables, figures, and listings. The role requires advanced biostatistics or epidemiology expertise and strong communication skills.

Conducts clinical data management activities for Phase I–III trials, including ongoing data review, reconciliation of third-party data and serious adverse events, clinical database user acceptance testing, database quality control, and documentation updates. Ensures compliance with ICH/GCP guidelines and delivery of quality work within required timelines.

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

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

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 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.

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.

Lead statistical programmer developing SAS code and ADaM-specified datasets, tables, listings, and graphs for clinical trials. Ensures quality, validation, documentation, inspection readiness, mentors programmers, manages timelines, participates in sponsor meetings, and follows regulatory and SOP requirements.

Lead statistical planning and delivery for clinical studies using R and RShiny, mentor biostatistics staff, prepare SAPs and programming specifications, perform quality control, support submissions and regulatory interactions, and develop/maintain R-based visualization apps and infrastructure.

Lead and mentor biostatistics teams for ophthalmology clinical trials across the study lifecycle. Oversee SAPs, statistical analyses, QA/reviews, regulatory interactions, programming specifications, and timelines. Support complex projects, DSMBs, proposal work, and ensure inspection readiness while providing statistical programming and technical leadership.