Jobs at Syneos Health

Lead programming activities for clinical trials, develop SAS code for statistical analysis, ensure quality outputs, manage multiple projects, and mentor programming personnel.

The Safety and PV Ops Specialist II maintains compliance with safety regulations, supports quality assurance activities, and manages safety database operations while ensuring training and proposal support for the Pharmacovigilance team.

The Principal Biostatistician mentors staff, oversees biostatistical work, develops training, prepares analysis plans, and ensures quality in statistical deliverables for clinical projects.

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 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 custom programming code using SAS to create statistical outputs, ensures quality standards, and manages programming documentation and team coordination while acting as a lead for programming tasks.

The role involves developing custom SAS programs for clinical data analysis, ensuring quality standards, collaborating with project teams, and mentoring junior programmers.

The Senior Clinical Programmer is responsible for programming, testing database designs, managing reporting tools, troubleshooting issues, and collaborating with teams to ensure compliance and data integrity in clinical programming tasks.

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.

The role involves programming using SAS and R, developing statistical outputs, managing project documentation, mentoring staff, and acting as the lead programmer for PK analysis in clinical trials.

The Principal Stat Programmer develops custom SAS code for clinical studies, ensuring quality outputs, managing project timelines, mentoring junior staff, and collaborating with project teams on clinical data analysis.

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.

Provide statistical support for clinical trials, prepare analysis plans, review programming specifications, coordinate biostatistics activities, and manage project deliverables.

Lead and support statistical activities across clinical trial lifecycles: prepare SAPs, review CRFs and database design, coordinate biostatistics and programming work, perform QC, support regulatory interactions, mentor staff, and contribute to proposals and study reporting.

The Senior/Principal Statistical Programmer develops programming code for statistical analysis, ensures output quality, manages project documentation, and leads programming activities while mentoring junior staff.

The role requires a Senior Statistical Programmer with expertise in R and R Shiny to create visualizations and work with clinical trial data, alongside managing multiple studies and effective communication.

The Sr Biostatistician will be responsible for statistical activities including SAP writing, mock shell creation, CSR review, and will need proficiency in R and SAS with experience in clinical trials and therapeutic areas.

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 TMF Document Assistant performs quality control of study documents, identifies quality issues, updates metadata in the eTMF system, and participates in training.