Senior Biostatistician
At a glance
Senior Data Science role at ICON. Remote, Poland · full-time.
Pay not stated Data Science salary
dataroles summary, based on the employer's posting.
What you'll do
- Lead statistical work across clinical studies, from straightforward designs through more complex trials
- Write analysis plans and define the specifications used to report study results
- Shape CRF statistical requirements and edit checks, then analyse trial data and explain the findings
- Review randomization plans and sample schemes, and join meetings to defend study bids
What you bring
- A master's or doctoral degree in biostatistics, statistics or a related field
- At least five years of biostatistics work, plus knowledge of statistical methods, therapeutic areas and drug development
- You can work independently, solve problems carefully and communicate with multidisciplinary teams
Who this fits
This senior role suits a biostatistician ready to lead study work and guide others. It is remote in Poland, and employment depends on your legal right to work there.
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.
As a Senior Biostatistician I at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will lead on biostatistics tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
- Serves as lead biostatistician for simple to complex clinical studies.
- Develops statistical analysis plans and reporting specifications.
- Responsible for statistical aspects of CRF design and edit specifications.
- Performs statistical analyses and interprets results for simple to complex clinical studies.
- Reviews simple to complex randomization specifications and dummy randomization schemes.
- Participates in bid defense meetings.
Your Profile:
You will have a strong foundation in biostatistics, with the experience to work independently and guide others.
Required qualifications and experience:
- Master's degree or Ph.D in Biostatistics, Statistics, or a related field with 5 or more years of biostatistical experience.
- Strong knowledge of multiple statistical and therapeutic areas, the drug development process, and statistical programming practices and procedures.
- Excellent problem-solving skills and attention to detail.
- Effective communication skills to collaborate with multidisciplinary teams.
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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