Job ID: 25101343
Location: Hyderabad, India (Hybrid)
Last Updated: August 28, 2025
Syneos Health® is a fully integrated biopharmaceutical solutions company, designed to accelerate customer success. We unite clinical development, medical affairs, and commercial expertise to deliver tailored solutions for today’s complex market.
With over 29,000 employees across 110 countries, we place both the customer and patient at the center of everything we do, focusing on innovation, efficiency, and streamlined collaboration.
Career Growth & Learning
Supportive management, structured career development, technical and therapeutic training.
Inclusive & Authentic Culture
Our Total Self culture promotes authenticity and belonging across all teams globally.
Employee Recognition & Rewards
A strong peer recognition and total rewards program supports our commitment to employee success.
Industry Impact
Supported 94% of all FDA-approved novel drugs in the last 5 years
Partnered on 95% of EMA-authorized products
Contributed to 200+ studies, across 73,000 sites and 675,000+ trial patients
As a Senior Biostatistician, you will lead and support statistical activities in clinical trials across various therapeutic areas. You will work cross-functionally to ensure timely and accurate statistical input for protocols, analyses, and regulatory submissions.
(Note: Specific tasks were not listed in the original job post. Below are standard expectations for this role.)
Develop and review Statistical Analysis Plans (SAPs), including mock tables, listings, and figures.
Provide statistical input to clinical study protocols and CRFs.
Conduct statistical analyses using SAS and/or R.
Ensure accuracy and quality in statistical deliverables.
Oversee the generation and validation of statistical outputs.
Interpret results and collaborate with clinical and regulatory teams.
Support responses to health authority questions or submissions.
Mentor junior statisticians and contribute to internal process improvements.
Ensure compliance with SOPs, ICH-GCP, and regulatory standards.
Though not listed, typical requirements include:
Education:
Master’s or Ph.D. in Biostatistics, Statistics, or related discipline.
Experience:
4–6 years of experience in clinical trial biostatistics (CRO or pharma setting preferred)
Proficiency in SAS programming and statistical methods
Knowledge of CDISC standards (SDTM, ADaM)
Familiarity with regulatory guidance (FDA, EMA)
Skills:
Strong analytical and communication skills
Team-oriented mindset with the ability to work independently
Attention to detail and commitment to data quality
Responsibilities may evolve depending on business needs.
Syneos Health may consider equivalent experience or education in lieu of formal qualifications.
This job posting does not constitute an employment contract.
Syneos Health complies with local and international labor laws, including the EU Equality Directive and Americans with Disabilities Act (ADA).
Reasonable accommodations will be provided when appropriate.
Not ready to apply? Join our Talent Network to stay connected.
At Syneos Health, we are committed to building a diverse, inclusive, and authentic workplace. If your background doesn’t align perfectly with every requirement, we encourage you to apply. We recognize transferable skills and value different career journeys.
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