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Sr-Principal Biostatistician - Oncology (Europe Only)

Syneos Health
Syneos Health
10-15 years
preferred by company
10 Feb. 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior / Principal Biostatistician – Oncology (Europe Only)

Updated: February 3, 2026
Location: London, United Kingdom (Europe-based candidates only)
Job ID: 25103095
Employment Type: Full-Time


About the Role

Syneos Health is seeking a highly experienced Senior or Principal Biostatistician specializing in oncology to support statistical analysis and clinical trial data management for Europe-based studies. This senior leadership role is ideal for candidates with a proven record in the pharmaceutical or CRO sector, delivering high-quality statistical oversight, mentoring biostatistics teams, and driving oncology study success from protocol development through to clinical study reports (CSRs).

The successful candidate will operate within a collaborative, patient-focused Clinical Development model, providing expert guidance on complex oncology trials, ensuring regulatory compliance, and applying best-in-class statistical practices to support clinical development programs.


Key Responsibilities

  • Serve as a subject matter expert in oncology biostatistics, mentoring and coaching junior biostatisticians and associates.

  • Oversee and direct statistical activities for assigned clinical trials, ensuring timely, accurate, and high-quality deliverables.

  • Prepare and review Statistical Analysis Plans (SAPs), tables, listings, and figures; develop mock-up displays as needed.

  • Lead statistical components of study protocols, including randomization schedules and contribution to clinical study reports.

  • Review annotated CRFs, database designs, and other study documentation to ensure alignment with protocol and regulatory standards.

  • Collaborate with cross-functional project teams, including clinical, regulatory, and programming personnel, to ensure study objectives are met.

  • Conduct verification, quality control, and review of statistical outputs to ensure consistency with SAPs and regulatory requirements.

  • Manage multiple complex projects, integrated analyses, and submissions, while adhering to timelines and study milestones.

  • Support regulatory interactions, including participation in Data Safety Monitoring Boards (DSMBs) and Data Monitoring Committees (DMCs) as needed.

  • Provide statistical programming support and oversee programming specifications for datasets, tables, listings, and figures.

  • Maintain comprehensive, inspection-ready project documentation and adhere to SOPs, WIs, and relevant regulatory guidelines (e.g., ICH).

  • Contribute to business development efforts, including proposals, budgets, and sponsor bid defense meetings.

  • Display flexibility and collaboration across multiple studies, contributing ideas, solutions, and expertise to team initiatives.


Required Qualifications & Experience

  • Location: Candidates must be based in Europe.

  • Education: Advanced degree in Biostatistics, Statistics, Mathematics, or related discipline (MS or PhD preferred).

  • Experience:

    • Minimum 10–15 years of biostatistics experience in the pharmaceutical, biotech, or CRO industry.

    • Proven experience in oncology clinical trials, including leading statistical analysis and reporting.

    • Demonstrated success mentoring or leading biostatistics teams.

    • Extensive knowledge of statistical methodologies, clinical trial design, and data analysis for oncology studies.

  • Proficiency with SAS programming, statistical software, and data visualization tools.

  • Familiarity with regulatory requirements and industry guidelines (ICH, EMA, FDA) for clinical trial data and statistical reporting.

  • Strong project management skills, including prioritization, timeline management, and resource allocation.

  • Excellent interpersonal, communication, and presentation skills for cross-functional and sponsor interactions.

  • Willingness to travel minimally for meetings and study-related activities within Europe.


Why Syneos Health

Syneos Health is a fully integrated biopharmaceutical solutions organization dedicated to accelerating the delivery of life-changing therapies worldwide. With 29,000 employees across 110 countries, we provide opportunities to work on innovative oncology programs, impacting the lives of thousands of patients globally.

We foster a Total Self culture, supporting diversity, equity, and inclusion while encouraging employees to bring their authentic selves to work. Professional development, mentorship, and a collaborative environment are central to our approach.


Additional Information

  • This job description provides a summary of the responsibilities; additional duties may be assigned based on organizational needs.

  • Equivalent combinations of education, skills, and experience will be considered.

  • Syneos Health is an equal opportunity employer and committed to compliance with local labor laws and regulations. Reasonable accommodations are provided to qualified individuals as required.


Job Summary:
This role is ideal for a senior oncology biostatistician with extensive leadership experience, capable of managing complex trials, mentoring teams, and contributing to high-impact European clinical research programs.