Jobs at Syneos Health

The Clinical Scientific Advisor supports clinical trial activities, builds relationships with KOLs, and ensures protocol execution. Requires 2+ years in clinical research, preferably in Neuroscience/Psychiatry.

Lead statistical programming for clinical trials using SAS to produce SDTM datasets, tables, listings, and figures. Ensure quality, validation, and regulatory-compliant documentation; mentor and direct other programmers; participate in sponsor meetings and study planning; manage multiple projects and timelines while following SOPs and ICH guidelines.

Develop and validate SAS programs to produce SDTM, ADaM, and TLF outputs per SAP/specs; ensure QC, documentation, and inspection readiness. Lead and mentor programmers, participate in sponsor meetings, provide CDISC/DEFINE.XML guidance, support ISS/ISE and safety/efficacy analyses, and contribute to SOPs and tooling. Minimal travel.

The Project Specialist at Syneos Health will collaborate on biopharmaceutical projects, support customer success, and contribute to clinical development initiatives within a diverse team.

Lead project-level non-CRF data management: define non-CRF data types, coordinate vendors and transfers, implement IXRS UAT, manage DTS/DTA/FFS and testing, ensure data delivery, oversee TMF and financials, report to sponsors, mentor staff, and maintain SOP compliance.

Lead statistical programmer using SAS to develop tables, listings, figures, and derived datasets per SAP and specifications. Validate outputs, maintain documentation, ensure regulatory compliance, mentor and direct other programmers, participate in sponsor meetings, manage multiple projects and timelines, and support inspection readiness. Minimal travel possible.

Provide regulatory expertise to support drug development and commercialization, advise on regulatory strategy and compliance, collaborate with clients and cross-functional teams to shape solutions across clinical programs.

The Safety & PV Specialist I is responsible for data entry and tracking of safety reports, maintaining compliance with SOPs, and conducting literature reviews related to safety in clinical trials.

The Sr. Statistical Programmer develops programming code using SAS to generate statistical outputs, ensures quality standards, manages multiple projects, and leads programming teams. Responsibilities include documentation, communication with teams, and mentoring programming personnel while participating in sponsor meetings.

The Senior HRIS Analyst manages Workday applications, drives HRIS projects, supports system optimization, and enhances user experience. They train staff, ensure data integrity, analyze needs for improvements, and collaborate with global teams.

The Principal Biostatistician in Clinical Pharmacology will lead statistical aspects of clinical studies, contribute to research design, and collaborate with teams to ensure drug development success.

Execute central report review activities to ensure patient safety, protocol/GCP/regulatory compliance, and data integrity. Review site and central monitoring documentation, document revisions and approvals in CTMS, identify and escalate serious issues, record observations and protocol deviations for action, assess report quality and trends, and participate in project meetings and training.