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ClinChoice

Junior Statistician - (Permanent Role)

Posted Yesterday
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Remote
Hiring Remotely in United States
Junior
Remote
Hiring Remotely in United States
Junior
Supports clinical trial statistical activities under senior guidance, including study design and analysis, statistical analysis plans, tables, listings, figures, data checks, clinical study reports, documentation, and statistical programming collaboration. Works with cross-functional clinical research teams while following SOPs, regulatory requirements, and applicable standards such as CDISC, SDTM, and ADaM.
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ClinChoice is a global full-service CRO committed to professional growth and a quality-driven “one-team” culture. We are seeking a Junior Statistician to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes.

We are seeking a motivated and detail-oriented Junior Statistician to join our team and support statistical activities across clinical research projects. The successful candidate will work closely with experienced statisticians, statistical programmers, data managers, and other cross-functional teams to support the planning, analysis, and reporting of clinical trial data.


Key Responsibilities
  • Support senior statisticians in the design and analysis of clinical studies.
  • Assist with statistical analysis plans (SAPs), table/listing/figure (TLF) specifications, and other statistical documentation.
  • Perform basic statistical analyses under appropriate guidance and supervision.
  • Support the review and interpretation of clinical trial data.
  • Assist with the preparation and review of statistical tables, listings, and figures.
  • Conduct data checks and identify discrepancies or potential data issues.
  • Support statistical programming activities and collaborate with statistical programmers.
  • Contribute to study reports, clinical study reports (CSRs), and other project documentation.
  • Maintain accurate and organized study documentation in accordance with project requirements and applicable guidelines.
  • Participate in project meetings and communicate progress, issues, and timelines effectively.
  • Follow company standard operating procedures (SOPs), project-specific procedures, and applicable regulatory requirements.
Qualifications
  • Master's degree in Statistics, Biostatistics, Mathematics, or a related quantitative discipline preferred.
  • Bachelor's degree with relevant experience may also be considered.
  • 0–2 years of experience in statistics, biostatistics, or clinical research.
  • Basic understanding of statistical concepts and methodologies.
  • Familiarity with clinical trial processes and pharmaceutical/biotech research is preferred.
  • Exposure to statistical software such as SAS, R, or Python is an advantage.
  • Good analytical, problem-solving, and organizational skills.
  • Strong attention to detail and ability to work effectively in a team environment.
  • Good written and verbal communication skills.
Preferred Experience
  • Exposure to clinical trial data and CDISC standards such as SDTM and ADaM.
  • Basic knowledge of clinical study design and statistical methods.
  • Experience working with statistical programming or clinical data is a plus.


What We Offer
  • Opportunity to work on global clinical research projects.
  • Exposure to experienced statisticians and cross-functional teams.
  • Opportunities for professional development and career growth.
  • Collaborative and learning-oriented work environment.


The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.           

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

#LI-TT1 #LI-Remote #senior #permanent


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