Job Description

At Clario, our purpose is to transform lives by unlocking better evidence. As a Biostatistician within our Cardiac team, you will play a critical role in delivering high‑quality statistical analyses that support cardiac safety evaluations and clinical trial outcomes. You will collaborate closely with cross‑functional scientific teams to ensure accurate, timely, and compliant statistical deliverables that advance our clients’ drug development programs.

What We Offer

• Competitive compensation

• Comprehensive medical, dental, and vision coverage

• 401(k) plan with company match

• Generous paid time off and paid holidays

• Fully remote work arrangement within the United States
  

What You’ll Be Doing

• Develop, test, execute, and maintain SAS and R programs for statistical analyses, including central tendency analysis, categorical analysis, and concentration‑QTc analysis

• Validate statistical results through double programming and independent verification

• Prepare tables, figures, and listings (TFLs) in accordance with approved statistical analysis plans

• Review final outputs and reports to ensure alignment with planned statistical methodologies

• Perform quality checks on CDISC‑formatted analysis datasets (ADaM)

• Support research programs by providing statistical results and insights to senior team members and department management

• Interpret and communicate statistical methodologies, results, and conclusions to Principal/Senior Principal Biostatisticians, Medical Writing, and Scientific Teams

• Train team members on standard operating procedures and standard statistical methodologies

• Drive process improvements to enhance operational efficiency and data quality

• Manage timelines, client commitments, and on‑time delivery for assigned projects

• Maintain accurate deliverable tracking, status updates, and milestone dates in team tracking tools

• Assist with the development, coordination, maintenance, and enforcement of quality standards, including SOPs, SWIs, playbooks, checklists, and templates.
  

What We Look For

• Master’s degree in Statistics, Mathematics, or a related discipline with at least 2 years of relevant industry experience, or Bachelor’s degree in Statistics, Mathematics, or a related discipline with at least 6 years of relevant industry experience

• Experience in clinical trials within a CRO or pharmaceutical research organization

• Strong proficiency in SAS or R programming

• Familiarity with statistical methodologies including ANOVA, t‑tests, regression, and linear mixed‑effects modeling

• Experience generating tables, figures, and listings (TFLs)

• Understanding of clinical protocols, statistical analysis plans, and the pharmaceutical drug development process

• Awareness of CDISC SDTM and ADaM standards

• Prior experience in statistical modeling for clinical trials, with a focus on QT modeling

• Strong analytical, organizational, and communication skills, with the ability to explain complex statistical concepts clearly

• Ability to work independently and collaboratively while adapting to changing priorities

• Proficiency with Windows and Microsoft Office applications

• Willingness to travel up to 50%, as required, and ability to perform computer‑based work for extended periods.

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life‑changing therapies to patients faster.

EEO Statement

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.