Jobs at Syneos Health

The role involves overseeing clinical trials, creating project plans, managing budgets, ensuring compliance with regulations, and developing recruitment strategies.

The Project Manager II coordinates clinical study timelines, collaborates with teams, ensures compliance with regulations, oversees operational aspects of trials, and develops recruitment strategies for successful enrollment.

Manage and coordinate clinical research studies, ensuring compliance with regulations, maintaining study documentation, and facilitating communication among stakeholders.

Provide administrative and logistical support for clinical trial supplies under the Clinical Trial Supplies Manager or Project Lead: assist distribution, resupply and return planning, support batch manufacturing and packaging record review, customs clearance, and inventory forecasting in collaboration with project teams and vendors.

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 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.

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 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 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.

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).