Principal Statistician – Rare Diseases Phase III and IV

🕒 August 26

🇫🇷 France – Remote

⏰ Full Time

🔴 Lead

✨ Principal

👻 Ghost score 33%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Serve as a statistical department resource and mentor biostatisticians • Oversee or develop training plans and materials; conduct training sessions • Direct activities of biostatistics personnel on assigned projects and independently review project work • Provide support across statistical tasks throughout the project lifecycle, from protocol to CSR • Prepare or oversee Statistical Analysis Plans and mock-up displays • Serve as Lead Biostatistician for protocol statistical aspects, randomization schedules, and clinical study report input • Create or review programming specifications for analysis datasets, tables, listings, and figures • Review SAS/R annotated CRFs, database design, and study documentation • Represent biostatistics on project teams and collaborate with departmental representatives • Conduct verification and quality control of project deliverables • Lead complex or multiple projects, including submissions and integrated analyses • Attend regulatory agency meetings or respond to questions regarding clinical trial statistical analyses • Manage schedules, priorities, timelines, milestones, and out-of-scope tasks across projects • Provide statistical programming support as needed • Participate in DSMB/DMC activities, including charter development and serving as an independent or voting statistician • Follow applicable SOPs, WIs, and relevant regulatory guidelines such as ICH • Maintain complete, current project and quality-control documentation for inspection readiness • Support business development through proposals, budgets, and sponsor bid defense meetings • Perform other work-related duties as assigned

🎯 Requirements

• Graduate degree in biostatistics or related discipline • Extensive experience in clinical trials or an equivalent combination of education and experience, demonstrated by the ability to lead multiple projects and programs of studies • Proficiency in R programming • Extensive knowledge of statistical design, analysis, relevant regulatory guidelines, and programming techniques utilized in clinical research • Ability to effectively communicate statistical concepts • Experience across all statistical tasks required to support clinical trials during the lifecycle of the project, from protocol to CSR • Experience with regulatory submissions preferred • Excellent written and verbal communication skills • Ability to read, write, speak, and understand English

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Minimal travel may be required