Clario hiring Associate Biostatistician • Remote (Work from Home) | Himalayas
ClarioCL

Associate Biostatistician

Clario is a leading healthcare research and technology company that enhances clinical trial management through comprehensive endpoint solutions and scientific expertise.

Clario

Employee count: 1001-5000

United States only
Create, test and maintain SAS codes used to create and/or validate statistical outputs for the cardiac safety statistical analysis; provide statistical support under supervision

Clario is a 50+ year old company that delivers industry leading clinical trial endpoint technology solutions. The future of clinical trials is vibrant, with new technologies revolutionizing what’s possible. From new trial modes to faster and integrated evidence and findings, our innovative clinical trial solutions mean we can unlock better evidence.

What we offer:

  • Competitive compensation

  • Medical, dental, and vision insurance beginning Day 1 of employment

  • Flexible work schedules

  • Attractive PTO plan

  • Engaging employee programs

  • Remote working

What you'll be doing:

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

  • Validate results of statistical analysis by double programming Prepare tables, figures, and listings for statistical analysis as outlined in the statistical analysis plan

  • Perform review of final outputs and reports as it relates to the planned statistical analysis

  • Perform quality checks on CDISC formatted analysis datasets (ADaM) Support research programs and provide research results to the senior team resources and/or department management Manage timelines and client commitments and ensure on-time delivery for assigned projects Inputs & maintains accurate deliverable status/dates, etc. team tracking tool

  • Assist with the development, coordination, maintainenance & enforcement of quality standard compliance, including creating SOPs, SWIs, Playbook/Checklists and Templates for team deliverables

  • Perform other duties, assignments, or special projects as needed

  • Provide interpretation of results/reports of statistical analysis including descriptions of methodologies and conclusions to the Principal/Sr. Principal Biostatistician, Medical Writing, and/or Scientific Team

  • Drive ideas for future analyses and data quality efforts Participate in Client discussions to communicate statistical methodologies used in the analysis

  • Demonstrate proficiency in understanding of team procedures & content/application within team's deliverables and alignment across the organization

What we look for:

  • A Master’s degree in Statistics, Mathematics or equivalent

  • Bachelor’s degree in Statistics, mathematics or equivalent with 3+ years of relevant industry experience.

  • Familiarity and experience with ANOVA, t-test, regression, and linear mixed-effects modeling.

  • Strong SAS or R programming skills.

  • Excellent verbal and written communication skills

  • Strong organization, analytical and communication skills

  • Experience with Windows and Microsoft Office products

  • Ability to learn quickly, function independently, and handle increasing levels of responsibility

  • Ability to work in a group setting and independently, adjusting to rapidly changing priorities

  • Experience with Windows and Microsoft Office products

  • Ability to learn quickly, function independently, and handle increasing levels of responsibility

  • Ability to work in a group setting and independently, adjusting to rapidly changing priorities

Working conditions:

Travel: 0-50%

Lifting: 0-25 lbs

Other: Computer work for long periods of time

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

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.

The Department Head has the discretion to hire personnel with a combination of experience and education, which may vary from the above listed qualifications.

This JOB description should not be deemed all-inclusive. Additional requirements and expectations may be assigned. At all times, employees are expected to adhere to company policies and company SOPs.

The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. The Company reserves the right to amend or change this job description to meet the needs of the Company. This job description and any attachments do not constitute or represent a contract.

About the job

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Job type

Full Time

Experience level

Entry-level

Location requirements

Hiring timezones

United States +/- 0 hours

About Clario

Learn more about Clario and their company culture.

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At Clario, we understand that our customers face challenges in conducting clinical trials that yield reliable evidence while ensuring safety, efficacy, and quality of life for patients. This is why we leverage our 50+ years of clinical trial data management expertise to drive innovation and deliver dependable solutions. Our primary aim is to empower pharmaceutical, biotech, and medical device companies to transform lives by providing the richest clinical evidence available.

We specialize in endpoint technologies and comprehensive management services for clinical trials, supporting over 26,000 studies in more than 100 countries. Our solutions integrate deep scientific expertise with advanced technology, ensuring accurate data collection and analysis. With our unmatched operational scale and global reach, we facilitate seamless trial execution, enhance patient engagement, and ensure adherence to regulatory standards. At the heart of our mission is a commitment to not only improve data reliability but also elevate the patient experience, making their health and well-being our top priority.

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