Senior Biostatistician

Reposted 17 Days Ago
Be an Early Applicant
3 Locations
In-Office
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
The Senior Biostatistician will lead statistical analyses for clinical trials, mentor junior team members, and manage client interactions while ensuring compliance with regulatory standards.
Summary Generated by Built In
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

Skills Required

  • Master's degree or Ph.D. in Biostatistics, Statistics, or related field
  • 6+ years of biostatistical experience in CRO, pharmaceutical, or biotech
  • Experience leading Phase II-III studies
  • Regulatory experience for NDA applications
  • Strong communication and leadership skills

ICON plc Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.

  • Healthcare Strength Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
  • Leave & Time Off Breadth Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
  • Retirement Support Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.

ICON plc Insights

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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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