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Senior Biostatistician

710 ICON India Central Services - IND · Bangalore, India

Clinical TrialsImported listingfull-time1 day ago

About The Role

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

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  • Serve as lead biostatistician for programs of studies, submissions, or on simple to complex individual studies
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  • Oversee statistical activities that support ICON’s interactions with clients and regulatory agencies
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  • Review and approve statistical methods sections of study protocols, statistical analysis plans, and statistical input to reports
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  • Program using SAS and/or R for inferential statistics
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  • Prepare and approve research proposals and budgets to provide statistical consulting and to conduct statistical analyses for clients
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  • Participate in bid defense meetings and make presentations at marketing meetings with prospective clients
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  • Mentor or provide support to junior statisticians
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  • Lead or partake in initiatives to improve internal processes or create new guidance

Your profile

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Master's degree OR Ph.D. in Biostatistics, Statistics, or a related field
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6+ years of biostatistical experience in either a CRO, pharmaceutical, or biotech company
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Experience leading Phase II-III studies, including client facing responsibilities, timeline management, and resource oversight
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Experience working in a clinical research organization preferred
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Regulatory experience (supporting and the handling of regulatory requests, for example: NDA applications)
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Advanced ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical studies
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Effective written and oral communication skills with demonstrated leadership ability
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Ability to prioritize with strong time management skills
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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

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