Jobs at Syneos Health

Leads statistical programming for clinical trials, using SAS to create and validate datasets, tables, listings, and graphs. Reviews specifications and study documents, ensures regulatory-quality documentation and inspection readiness, resolves discrepancies, manages timelines across projects, and directs programming activities. Participates in sponsor meetings, mentors programmers, reviews deliverables, and supports training and project initiatives.

Leads clinical programming for multiple concurrent studies using Medidata Rave and related clinical systems. Develops, validates, migrates, and maintains study databases, custom functions, edit checks, integrations, reports, and documentation. Provides technical oversight, senior quality review, audit support, vendor management, resource planning, budgeting, and change-order management. Mentors clinical programmers, coordinates project teams, supports sponsor interactions, and oversees programming operations across large study programs.

Leads Biometrics Optimization projects, including clinical research procedures, training programs, certification management, documentation, governance, and continuous improvement. Oversees project timelines, risks, metrics, dashboards, financial performance, and cross-functional delivery. Mentors staff and may manage direct and indirect reports. Supports global work transitions, regulatory compliance, executive reporting, and operational initiatives across Biometrics functions.

Develop and maintain SAS programs for ADaM analysis datasets, tables, and figures in clinical research. Provide statistical programming support, troubleshoot issues, ensure data integrity, and collaborate with statisticians and clients. Improve programming processes, manage multiple projects, and mentor junior professionals while maintaining compliance with statistical standards and quality requirements.

Leads statistical programming for clinical trial deliverables, developing and validating SAS or other programs for SDTM, ADaM, tables, listings, figures, and derived datasets. Oversees concurrent projects, timelines, quality control, documentation, regulatory compliance, and sponsor communications. Acts as a technical expert in CDISC standards, mentors programmers, reviews specifications and deliverables, supports process improvements, and contributes to programming tools, SOPs, and training.

Leads clinical data management services for assigned projects, coordinating data management teams and ensuring delivery of study milestones, documentation, quality, and regulatory compliance. Manages project plans, resources, finances, sponsor communications, audits, training, and TMF filing. Requires end-to-end clinical data management experience, client-facing study leadership, Rave CDMS expertise, and strong project management skills. Oncology and Phase 1 experience are preferred. Travel may be required up to 25%.

Leads clinical development operations strategy, planning, process optimization, quality compliance, project management standards, resource allocation, metrics, and continuous improvement. Manages regional and senior staff, supports hiring and development, oversees SOPs and work instructions, coordinates cross-functional operations, and ensures adherence to GCP, ICH, regulatory, budget, schedule, and risk requirements. Travel may be required up to 25%.

Develops and advises on risk-based central monitoring strategies for clinical studies. The role leads risk assessments, supports Risk Assessment Categorization Tool processes, evaluates centralized statistical monitoring and data-quality risks, defines quality tolerance limits, and facilitates cross-functional and sponsor reviews. It also provides training, mentoring, inspection-readiness support, budget and scope oversight, risk escalation, and occasional business-development assistance while ensuring compliance with ICH/GCP, protocol, country regulations, and applicable good pharmacoepidemiology practices.

Leads clinical statistical programming across multiple complex projects using SAS to create and validate ADaM datasets, tables, listings, and figures. Develops specifications, ensures CDISC and regulatory compliance, reviews clinical documentation, manages timelines, and supports inspection readiness. Serves as the lead programmer and technical expert, directing programming teams, mentoring staff, contributing to tools and SOPs, and participating in sponsor and bid defense meetings.

Leads statistical programming for clinical trials, developing and validating SAS outputs, datasets, tables, listings, and figures across safety and efficacy data. Creates specifications, ensures CDISC compliance, maintains inspection-ready documentation, manages concurrent deliverables, mentors programmers, supports sponsor meetings, and provides technical expertise in SDTM, ADaM, TLF, ISS, ISE, and regulatory submission requirements.

Leads statistical programming activities across complex clinical trial projects. Develops and validates SAS programs, datasets, tables, listings, and graphs; ensures quality, regulatory compliance, and inspection readiness. Oversees timelines, resolves discrepancies, supports sponsor meetings, mentors programmers, and provides technical expertise in CDISC standards, SDTM, ADaM, and regulatory submissions. Contributes to SOPs, programming tools, training, and standards compliance reviews while coordinating concurrent deliverables.

Leads statistical programming for clinical trials across Phases I–IV. Develops and validates SDTM and ADaM datasets, generates tables, listings, and figures, prepares Define-XML and reviewer guides, supports safety and efficacy analyses, and contributes to regulatory e-submissions. Collaborates across functions, leads multiple studies, ensures CDISC compliance, and provides senior-level review and project leadership in therapeutic areas such as oncology and neurology.

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.

Manages site contract and budget processes for clinical trials, including preparing, negotiating, reviewing, executing, tracking, and archiving agreements. Coordinates with legal, finance, clinical operations, sponsors, vendors, investigators, and sites to resolve issues and meet start-up timelines. Maintains contract databases, templates, training materials, and SOP compliance; monitors financial details, supports quality assurance, mentors junior staff, and communicates contract status across teams.

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.

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.