Biostatistician

Systimmune

$80K — $140K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Biostatistics, Statistics, or a related quantitative field
  • At least 1 year of industry experience in biostatistics within pharmaceutical, biotech, or CRO settings
  • Hands-on experience supporting clinical trials (any phase)
  • Proficiency in statistical programming (R and/or SAS)
  • Understanding of clinical trial design, endpoints, and regulatory expectations

Responsibilities

  • Support statistical activities for clinical trials across Phase 1 to Phase 3 studies
  • Develop statistical analysis plan
  • Contribute to study design, including sample size estimation and statistical methodology
  • Collaborate with clinical, data management, and programming teams to ensure data integrity and analysis accuracy
  • Work with global teams, including close collaboration with colleagues in China
  • Assist in interpretation of statistical results and communicate findings clearly to cross-functional stakeholders

Benefits

  • 100% paid employee premiums for medical/dental/vision
  • Short-term and long-term disability coverage
  • 401(k) plan with a 50% company match up to 3% and a 5-year vesting schedule
  • 15 PTO days per year plus sick leave and 11 paid holidays
  • Opportunities for professional development and growth
Full Job Description
We are seeking a Biostatistician to support clinical trial programs across Phase 1 through Phase 3 studies. This is an early-career role designed for candidates with a strong statistical foundation and initial industry experience who are looking to deepen their exposure to clinical development.

You will work closely with cross-functional teams, including clinical, regulatory, and international colleagues, to contribute to statistical analyses that inform decision-making across the clinical pipeline.

This position is full-time onsite and can be located in Redmond, WA; Sugarland, TX; or Princeton, NJ.

Key Responsibilities
  • Support statistical activities for clinical trials across Phase 1 to Phase 3 studies
  • Develop statistical analysis plan
  • Contribute to study design, including sample size estimation and statistical methodology
  • Collaborate with clinical, data management, and programming teams to ensure data integrity and analysis accuracy
  • Work with global teams, including close collaboration with colleagues in China
  • Assist in interpretation of statistical results and communicate findings clearly to cross-functional stakeholders


Qualifications
  • PhD in Biostatistics, Statistics, or a related quantitative field
  • At least 1 year of industry experience in biostatistics within pharmaceutical, biotech, or CRO settings
  • Hands-on experience supporting clinical trials (any phase)
  • Proficiency in statistical programming (R and/or SAS)
  • Understanding of clinical trial design, endpoints, and regulatory expectations

Compensation and Benefits:
The expected base salary range for this position is $80,000 - $140,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.

SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.

We offer an opportunity for you to learn and grow while making significant contributions to the company's success.

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