Jobs at Syneos Health

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 Senior Statistical Programmer develops programming codes using SAS for data analysis, leads programming activities, ensures quality standards, and manages project documentation and timelines, while mentoring junior programmers and communicating with various stakeholders.

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.

Lead statistical programming tasks including developing custom code using SAS, ensuring output quality, and mentoring junior programmers. Manage multiple projects, maintain documentation, and engage in sponsor meetings.

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.

The Sr Statistical Programmer develops programming code to generate datasets and graphical outputs, ensuring quality and compliance with specifications. They lead programming activities, manage project timelines, and mentor junior staff, while facilitating effective communication and documentation throughout the project lifecycle.

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 involves developing SAS programming code for clinical studies, validating outputs, and managing project timelines. Responsibilities include mentoring junior programmers and contributing technical expertise in CDISC standards.

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.

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 Statistical Programmer leads programming activities, develops SAS code for analysis tables, ensures data quality, manages projects, mentors staff, and communicates with stakeholders.

The Principal Statistical Programmer leads programming efforts, develops custom code, manages project timelines, ensures quality outputs, and mentors junior programmers. They navigate regulatory standards and collaborate with cross-functional teams for clinical projects.

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