Junior Statistician - (Permanent Role)

Posted 2 Days Ago
Be an Early Applicant
Hiring Remotely in United States
Remote
Junior
Pharmaceutical
The Role
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.
Summary Generated by Built In

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


Skills Required

  • Bachelor's degree in Statistics, Biostatistics, Mathematics, or a related quantitative discipline
  • 0-2 years of experience in statistics, biostatistics, or clinical research
  • Basic understanding of statistical concepts and methodologies
  • 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
  • Master's degree in Statistics, Biostatistics, Mathematics, or a related quantitative discipline
  • Familiarity with clinical trial processes and pharmaceutical or biotechnology research
  • Exposure to SAS, R, or Python
  • Exposure to clinical trial data and CDISC standards such as SDTM and ADaM
  • Basic knowledge of clinical study design and statistical methods
  • Experience with statistical programming or clinical data

ClinChoice Compensation & Benefits Highlights

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

  • Flexible Benefits Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
  • Leave & Time Off Breadth Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
  • Healthcare Strength Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.

ClinChoice Insights

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The Company
HQ: Fort Washington, PA
5,000 Employees
Year Founded: 1995

What We Do

ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.

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