Senior Biostatistician
At a glance
Senior Data Science role at ICON. India, Bangalore · full-time.
Pay not stated Data Science salary
dataroles summary, based on the employer's posting.
What you'll do
- Lead statistical work for study programs, submissions or individual trials ranging from straightforward to complex
- Direct statistical support for discussions with clients and regulatory agencies
- Check and sign off on statistical methods in protocols, analysis plans and study reports
- Use SAS or R for inferential analyses, and prepare client proposals with budgets
- Take part in bid defenses, present to prospective clients, guide junior statisticians and improve internal processes
What you bring
- A master’s degree or Ph.D. in biostatistics, statistics or a related field
- At least six years in biostatistics at a CRO, pharmaceutical company or biotech firm
- Experience leading Phase II, III studies, including client work, timeline control and resource oversight
- Advanced ability to plan and monitor statistical work across several clinical studies
Who this fits
This role suits a senior biostatistician comfortable leading studies and handling client-facing work. It can be based in an office or from home in India. You must be authorized to work in India.
From the employer
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
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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