Principal Biostatistician – Sponsor Dedicated

Syneos Health

Principal Biostatistician providing statistical support for clinical trials at Syneos Health. Collaborating with teams to ensure timely completion of high quality work.

Posted 7/28/2026full-timeRemote • 🇫🇷 FranceLeadWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in biostatistics and statistical programming, with a strong focus on clinical trials, statistical analysis plans, and regulatory compliance. Proficient in managing project timelines and coordinating biostatistics teams while ensuring high-quality deliverables.

Highest-signal resume keywords

BiostatisticsStatistical ProgrammingClinical TrialsSAS ProgrammingStatistical Analysis Plans

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Statistical DesignData AnalysisProgramming ProficiencyQuality ControlProject Documentation

Soft Skills

Excellent Communication SkillsTeam CollaborationCoaching and Mentoring

Tools & Technologies

SASStatistical Software

Industry Keywords

ICH GuidelinesClinical ResearchData Safety MonitoringRegulatory GuidelinesBiostatistics Protocols

About the role

Key responsibilities & impact

Provides support across all assigned statistical tasks during the lifecycle of the project, from protocol to CSR
Prepares Statistical Analysis Plans (SAPs)
May be responsible for the statistical aspects of the protocol
Coordinates the activities of other biostatistics and statistical programming personnel
Creates or reviews programming specifications for analysis datasets, tables, listings, and figures
Reviews SAS annotated case report forms (CRFs), database design, and other study documentation
Conducts and participates in verification and quality control of project deliverables
Implements company objectives, and create alternative solutions to address business and operational challenges
Serves as biostatistics representative on project teams
Manages scheduling and time constraints across multiple projects
Monitors progress on study activities against agreed upon milestones
Provides statistical programming support as needed
May participate in Data Safety Monitoring Board and/or Data Monitoring Committee activities
Follows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH)
Maintains well organized, complete, and up-to-date project documentation
Displays willingness to work with others and assists with projects and initiatives as necessary
Supports business development activities by contributing to proposals, budgets
Coaches and mentors other Biostatistics staff
Performs other work-related duties as assigned

Requirements

What you’ll need

Graduate degree in biostatistics or related discipline
Moderate experience in clinical trials or an equivalent combination of education and experience
Proficiency in programming
Ability to apply knowledge of statistical design, analysis, relevant regulatory guidelines, and programming techniques utilized in clinical research
Excellent written and verbal communication skills
Ability to read, write, speak, and understand English

Benefits

Comp & perks

We are passionate about developing our people, through career development and progression
Supportive and engaged line management
Technical and therapeutic area training
Peer recognition and total rewards program
Committed to building an inclusive culture – where you can authentically be yourself
Driven to Deliver – captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life