Job Description – Sr Biostatistician
Company: Syneos Health®
Location: [Insert location if applicable]
Department: Clinical Development
About Syneos Health
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. By combining clinical, medical affairs, and commercial expertise, we deliver innovative solutions that address today’s complex healthcare challenges.
Global presence: 29,000 employees across 110 countries
Impact: Collaborated on 94% of all FDA-approved drugs and 95% of EMA-authorized products in the past 5 years
Mission: Placing customers and patients at the center of everything we do, while streamlining processes to make working with us—and for us—simpler and more rewarding
Work Here Matters Everywhere.
Why Join Us
At Syneos Health, we are committed to:
Career growth & development: Ongoing technical, therapeutic, and leadership training
Supportive culture: Engaged line management, peer recognition, and a comprehensive rewards program
Total Self culture: Encouraging authenticity and inclusivity in the workplace
Diversity & belonging: Bringing together diverse perspectives to foster innovation and ensure everyone feels they belong
Role Overview – Sr Biostatistician
As a Senior Biostatistician, you will play a pivotal role in clinical development by providing statistical expertise and leadership across clinical studies. You will collaborate with cross-functional teams to design, analyze, and interpret study data, ensuring scientific integrity and regulatory compliance.
Key Responsibilities
Provide statistical input into study design, protocol development, and analysis plans
Perform statistical analyses and ensure accuracy, efficiency, and compliance with regulatory standards
Interpret study results and contribute to clinical study reports, publications, and regulatory submissions
Collaborate with cross-functional teams including clinical, medical, and programming colleagues
Actively contribute to process improvement initiatives and support innovation in statistical methodology
Mentor and provide technical guidance to junior statisticians and programming staff
Qualifications
Advanced degree (Master’s or Ph.D.) in Biostatistics, Statistics, or a related field
Strong knowledge of statistical methods for clinical trials
Proficiency in statistical programming software (e.g., SAS, R)
Excellent communication and problem-solving skills
Ability to work collaboratively in a dynamic, fast-paced environment
Prior experience in the pharmaceutical, CRO, or healthcare industry preferred
Additional Information
Responsibilities listed are not exhaustive; other tasks may be assigned as needed
Equivalent skills, education, and experience will be considered
The role complies with all relevant global employment regulations, including the EU Equality Directive and ADA reasonable accommodation requirements
How to Apply
[Apply Here]
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