Job Description

Job Description

Job Description

About Cleerly

We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location.

Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly's solutions are supported by more than a decade of performing some of the world's largest clinical trials to identify important findings beyond symptoms that increase a person's risk of heart attacks.

At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description.

About the Opportunity

Under the guidance of the Director of Biometrics and Chief Medical Officer, perform intermediate and advanced level statistical analysis and programming for a broad range of medical research projects. Collaborate closely with a cross-functional project team, medical affairs, physicians, regulatory, product development, evidence generation, market access and reimbursement, and the core laboratory with regard to statistical aspects of each project. Demonstrate expertise in determination and implementation of statistical methodology and interpretation of statistical analysis results.

TTC: $237,000 - $250,000

*Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.). We hire employees anywhere within the United States and account for geography when determining base salary.

Responsibilities

• Collaboration, communication, leadership, and project management

  • Collaborate effectively with evidence generation, medical personnel, and external clinical collaborators.

  • Collaborate effectively with clinical to translate clinical questions and objectives into measurable statistics and hypotheses.

  • Contribute constructively to project discussions in team meetings.

  • Demonstrate excellent written and oral proficiency in the English language.

  • Adhere to the standard operating procedures (SOPs) and best practices of Cleerly as they apply to documentation and validation of research methodology.

  • Function independently and manage multiple simultaneous project responsibilities and deadlines.

  • Take initiative to complete project-specific responsibilities with minimal to no supervision.

  • Demonstrate ability to multitask and meet deadlines.

  • Build documentation and organizational skills to effectively return to a project or manuscript after long intervals.

• Statistical analysis planning, generation, and interpretation
  • Perform intermediate and advance-level statistical analysis at all phases of a research project, from protocol development and study design through final analysis and reporting and interpretation of results and manuscript and abstract submission & revisions.
  • Evaluate research studies and recommend statistical procedures, including, but not limited to, hypothesis tests, regression models and multivariate analysis to analyze the data.
  • Contribute meaningfully to discussions of analyses and identify next steps for analyses.
  • Prepare statistical analysis plans independently.
  • Prepare comprehensive statistical reports to communicate findings.
  • Prepare statistical components of presentations, abstracts, study protocols, regulatory submissions, and manuscripts.
  • Learn new statistical methods as needed, and apply new skills to future projects.
  • Perform intermediate and advanced statistical analyses, including but not limited to generating descriptive and test statistics, and performing high-level statistical modeling.
  • Check results for accuracy and consistency.
  • Demonstrate clinical/statistical areas of expertise and serve as resource in this area.
• Programming and data documentation
  • Program and develop analysis datasets using SAS; combine multiple disparate raw data sets, execute standard cleaning and quality control procedures, and derive analytic variables as required.
  • Demonstrate good programming practices through proper documentation, commenting, and readability.
  • Perform complex programming using advanced options in SAS procedures and macros with increasing efficiency.
  • Participate actively in designing and validating analysis data sets, programs, and statistical output products (tables, listings, figures).
  • Perform appropriate and adequate code checks to ensure accuracy of results.
• Other Responsibilities
  • As part of a new startup with a highly collaborative culture, perform other related duties and "pitch in" where needed. In the early stages, these duties may include administrative operations and data management support.

Requirements

• Position requires a minimum of a Doctoral degree in (bio) statistics or related field and 8 years of relevant experience, or a Master's degree in (bio) statistics or related field and 12 years relevant experience.
• Contribution to analysis of clinical research projects, and/or participation in preparation of academic manuscripts, regulatory submissions, or other written summaries of analysis results.
• Experience with development and execution of statistical analysis plans and thorough experience with SAS including data manipulation and procedures for data analysis (proc univariate, means, freq, t-test, genmod, lifetest, proc phreg, logistic).
• Experience with statistical analysis of time-to-event data with censoring, multivariate analysis of predictors of time-to-event data, continuous data, and binary outcomes. Experience with ROC/AUC analyses.
• Experience with repeated measures data is a plus.
• Experience in the diagnostic or therapeutic medical device field strongly preferred.
• Solid command of the English language is required.
• Energy and enthusiasm consistent with working for a startup; strong technical presentation skills; strong organizational skills; ability to remain organized and productive in a fast-paced work environment with competing priorities; work independently, diligently, and efficiently on assigned tasks and projects, and collaborate seamlessly with colleagues from other technical teams.
• Desirable experience includes knowledge of cardiovascular imaging and clinical data.

Working at Cleerly takes HEART. Discover our Core Values:

• H: Humility - be a servant leader
• E: Excellence - deliver world-changing results
• A: Accountability - do what you say; expect the same from others
• R: Remarkable - inspire & innovate with impact
• T: Teamwork - together we win

Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company.

OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation.

By submitting your application, you agree to receive SMS messages from Cleerly recruiters throughout the interview process. Message frequency may vary. Message and data rates may apply. You can STOP messaging by sending STOP and get more help by sending HELP. For more information see our Privacy Policy (-policy). All official emails will come from @cleerlyhealth.com email accounts.

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