This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Biostatistician based in India.
This role offers the opportunity to play a critical part in the development and regulatory approval of innovative diagnostic solutions that support better patient outcomes worldwide. You will provide expert statistical leadership across the full product lifecycle, from study design and data analysis to regulatory submissions and post-study reporting. Working within a global, multidisciplinary environment, you will collaborate with clinical, scientific, regulatory, and engineering teams to transform complex data into actionable insights. The position combines technical rigor, scientific impact, and strategic influence, making it ideal for an experienced biostatistician who thrives in regulated healthcare settings. You will contribute to cutting-edge diagnostic advancements across infectious diseases, hematology, and oncology while helping shape best practices and statistical standards. This is a high-visibility role with meaningful opportunities to drive innovation and improve healthcare outcomes.
Accountabilities
As a Senior Biostatistician, you will provide statistical expertise across clinical and analytical studies, ensuring robust study design, accurate analysis, and regulatory compliance throughout the development of diagnostic products.
- Lead end-to-end statistical support for clinical studies, including study design, sample size determination, analysis, interpretation, and reporting.
- Apply advanced statistical methodologies such as multivariate analysis, classification techniques, survival analysis, and general linear modeling to support product development.
- Develop and author statistical sections of clinical protocols, statistical analysis plans, clinical study reports, and regulatory submission documents.
- Provide expert guidance on study design considerations, statistical risks, sampling strategies, and power calculations.
- Support analytical performance studies including precision, reproducibility, method comparison, linearity, accuracy, limit of detection, inclusivity, exclusivity, and interference assessments.
- Serve as a key statistical contact for regulatory inquiries and contribute to interactions with regulatory agencies.
- Review and improve standard operating procedures while delivering statistical training and knowledge-sharing initiatives across teams.
- Participate in audits and ensure statistical activities meet regulatory and quality standards.
Requirements
The ideal candidate brings strong biostatistical expertise, regulatory knowledge, and experience supporting clinical studies within highly regulated healthcare or diagnostics environments.
- Bachelor's degree in Statistics or Biostatistics with 8+ years of experience, or Master's degree with 6-8 years of experience, or PhD with 4+ years of experience.
- Proven experience as a lead statistician supporting IVD, medical device, imaging, or related clinical studies in regulated environments.
- Strong understanding of global regulatory frameworks and industry standards, including FDA, CE-IVDR, WHO, CLSI, and related guidelines.
- Proficiency with statistical and analytical tools such as SAS, R, Python, Minitab, and Excel.
- Experience designing and analyzing clinical studies, including regulatory submission support.
- Ability to translate complex scientific, engineering, and business challenges into practical statistical approaches.
- Excellent written and verbal communication skills, including the ability to present technical findings to non-statistical stakeholders.
- Strong analytical thinking, attention to detail, and problem-solving capabilities.
- Experience supporting regulatory submissions and interactions with regulatory authorities is highly desirable.
Benefits
- Competitive compensation and comprehensive benefits package.
- Remote working flexibility with access to global teams and projects.
- Opportunity to contribute to life-changing healthcare and diagnostic innovations.
- Exposure to cutting-edge technologies and scientific advancements in diagnostics and biotechnology.
- Collaborative and inclusive work environment that values continuous improvement and professional growth.
- Learning, development, and career advancement opportunities within a global organization.
- Paid time off, health and wellness programs, and additional employee support benefits.
- Opportunity to work alongside multidisciplinary experts across clinical, scientific, regulatory, and technical domains.
How Jobgether Works
We use an
AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Why Apply Through Jobgether
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
