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ICON

Senior Biostatistician

India, Bangalore · India, Trivandrum · India, Chennai

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hirly's read of this role

Seniority
Senior
Country
IN
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

  • Senior Biostatistician I / II - India - Office or Home
  • ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Senior Biostatistician to join our diverse and dynamic team. As a Senior Biostatistician at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing:

Serve as lead biostatistician for programs of studies, submissions, or on simple to complex individual studies

Oversee statistical activities that support ICON’s interactions with clients and regulatory agencies

Review and approve statistical methods sections of study protocols, statistical analysis plans, and statistical input to reports

Program using SAS and/or R for inferential statistics

Prepare and approve research proposals and budgets to provide statistical consulting and to conduct statistical analyses for clients

Participate in bid defense meetings and make presentations at marketing meetings with prospective clients

Mentor or provide support to junior statisticians

Lead or partake in initiatives to improve internal processes or create new guidance

Your profile:

Master's degree OR Ph.D. in Biostatistics, Statistics, or a related field

6+ years of biostatistical experience in either a CRO, pharmaceutical, or biotech company

Experience leading Phase II-III studies, including client facing responsibilities, timeline management, and resource oversight

Experience working in a clinical research organization preferred

Regulatory experience (supporting and the handling of regulatory requests, for example: NDA applications)

Advanced ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical studies

Effective written and oral communication skills with demonstrated leadership ability

Ability to prioritize with strong time management skills

#LI-KT1

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .

Are you a current ICON Employee? Please click here to apply

Original posting on ICON's site ↗

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