Senior Biostatistician
At a glance
Senior Data Science role at Fortrea. Remote, Poland · full-time.
Pay not stated Data Science salary
dataroles summary, based on the employer's posting.
What you'll do
- Set statistical approaches for clinical trials across therapeutic areas and shape analysis plans around each study’s objectives
- Use SAS to run analyses, then prepare reports that present the study findings
- Advise study teams on methods, sample-size choices and trial design, and resolve statistical questions across projects
- Check statistical outputs for accuracy and completeness
What you bring
- At least five years as a biostatistician at a CRO, biotech or pharmaceutical company
- A master’s or doctoral degree in biostatistics, statistics or a related subject
- Strong clinical-trial statistics knowledge, CDISC expertise and hands-on SAS skills, including debugging programs
- Professional work with SDTM, ADaM and TFL deliverables
Who this fits
This senior role suits an experienced biostatistician who can work independently and explain complex findings to nontechnical audiences. It is fully home-based for candidates in listed EMEA locations.
From the employer
Fortrea is looking for Senior Biostatistician to join our sponsor dedicated team
As a Senior Biostatistician at Fortrea, you will play a crucial role in the design, analysis, and interpretation of clinical trials, directly impacting the development of innovative therapies and treatments. Supported by a diverse team of research professionals, you will collaborate closely with study teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis.
Your Responsibilities:
Design and implement statistical strategies for clinical trials within various therapeutic areas.
Develop statistical analysis plans, ensuring their appropriateness for study objectives.
Perform statistical programming tasks using SAS for analyses and generate study reports.
Collaborate with cross-functional study teams to contribute statistical expertise and guidance.
Provide expertise on statistical methodology, sample size calculations, and innovative trial design.
Ensure the quality and integrity of statistical deliverables.
Oversight of all the statistical queries on multiple projects.
Your experience and qualifications:
Minimum of 5 years (Senior) of experience as a Biostatistician within a CRO, biotech or pharmaceutical company.
Solid understanding of statistical methods commonly used in clinical trials, including advanced concepts.
Extensive knowledge of CDISC standards.
Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs
Proven professional experience with SDTMs, ADaM datasets and TFLs
Strong knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards.
Excellent communication skills, with the ability to effectively collaborate and present complex data to non-technical audiences.
Advanced degree (Ph.D. or Master’s) in Biostatistics, Statistics, or a related field.
Demonstrated ability to work independently, utilize problem-solving skills, and make sound decisions.
What you can expect from us:
Pioneering Research: Join a CRO at the forefront of clinical trials within multiple therapeutic areas.
Career Growth: Expand your skill set and broaden your expertise in a supportive and environment, with numerous opportunities for career advancement.
Impactful Work: Contribute directly to the development of groundbreaking therapies and treatments, improving the lives of patients worldwide.
Competitive Compensation: We offer a competitive salary package, comprehensive benefits, and a rewarding bonus structure.
Life-Style: Flexibility to work remotely from anywhere, promoting a healthy work-life balance.
You can be 100% home-based in any of the EMEA locations listed on this ad
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.
Fortrea is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement.
If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact:
taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
Learn more about our EEO & Accommodations request here.
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