Jobs at Syneos Health

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.

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

The Regulatory Consultant will support global regulatory CMC for marketed small molecule products, preparing documentation and collaborating with cross-functional teams on submissions.

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.

Develop persuasive, client-focused proposals by collaborating with BD, medical, finance and functional teams; conduct qualitative and quantitative research; produce high-quality, branded deliverables; manage stakeholder communication and timelines to meet deadlines.

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 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.

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

Lead and deliver high-complexity pre-award feasibility assessments for global clinical trials across therapeutic areas. Independently analyze site-level data, prepare presentations/reports, support bid defenses, liaise with internal stakeholders, mentor junior staff, and contribute to process and data asset development to support RFPs and feasibility strategy.

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.

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.

The R Statistical Programmer prepares custom programming code using R, validates outputs, adheres to regulatory guidelines, leads programming activities, mentors colleagues, and ensures timely delivery of project deliverables.

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.