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ReCor Medical

Renal denervation system using ultrasound

Clinical Programmer 2

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timePalo Alto, CA, USA$122.9k - $132.8k /yrHybrid

About the Job

Requirements

  • A master's degree in computer science, data science, statistics, life sciences, or a related field with at least 1 year of experience; or a bachelor's degree in these fields with at least 2 years of professional experience in clinical programming, data visualization, business intelligence, or analytics roles.
  • Strong proficiency in R and/or SAS, with experience in other relevant programming languages and tools such as Python and SQL.
  • Ability to identify and resolve performance bottlenecks and optimize code for efficiency and scalability.
  • Experience extracting, cleaning, transforming, and loading data from diverse sources, managing datasets, and ensuring data quality and integrity.
  • Understanding of clinical trial processes and data flow from study setup to database lock.
  • Problem-solving and analytical skills, including the ability to translate complex requirements into efficient programming solutions.
  • Experience with version control systems such as Git and collaborative development practices.
  • Ability to mentor junior team members, conduct code reviews, and provide technical guidance.
  • Written and verbal communication skills, including the ability to explain technical concepts to non-technical stakeholders.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Commitment to continuous learning and staying updated with emerging trends in clinical programming and data analysis.

Responsibilities

  • Design, develop, validate, and maintain complex programs to support clinical trial data management processes, including data integration, transformation, and analysis using R, SAS, or other relevant programming languages.
  • Perform advanced data analysis and generate complex reports, tables, listings, and figures to support clinical trial data review, statistical analysis, regulatory submissions, and operational decision-making.
  • Develop and maintain tools for tracking study progress, site performance, and other key operational metrics; generate regular reports and dashboards to provide insights into clinical trial operations.
  • Collaborate with cross-functional teams to implement statistical analysis plans and design programming solutions that address specific project requirements.
  • Troubleshoot complex data issues and propose solutions to ensure data integrity and quality throughout the clinical development process.
  • Conduct programming peer reviews, provide technical guidance, and mentor junior programmers to ensure code quality and adherence to standards.
  • Participate in version control using Git and maintain comprehensive documentation for scripts, packages, and applications.
  • Contribute to study documentation, including programming specifications and data management plans.
  • Lead process improvement initiatives to enhance efficiency and quality in clinical programming activities.
  • Stay abreast of emerging trends, technologies, and industry standards such as CDISC in clinical programming and data management, implement improvements as appropriate, and assist in preparing for regulatory audits and inspections.
  • Perform other duties as assigned.

Desired Qualifications

  • Working knowledge of clinical trial data standards such as CDISC SDTM and ADaM.
  • Experience with or understanding of clinical trial operations and associated metrics.
  • Familiarity with tools and techniques for visualizing operational data and creating interactive dashboards, such as Tableau and Power BI.
  • Experience with data visualization tools such as Power BI and Tableau.
  • Proficiency in version control systems such as Git and collaborative development practices.
  • Experience mentoring junior programmers and conducting code reviews.
  • Familiarity with cloud-based data platforms and integration technologies.
  • Experience with software validation per FDA guidelines.
  • Knowledge of machine learning or advanced analytics techniques applicable to clinical data.

About the Company

ReCor Medical

Renal denervation system using ultrasound

ReCor Medical develops the Paradise System, a renal denervation platform that uses non-focused ultrasound to treat hypertension. The device delivers ultrasound energy to the kidney region to disrupt renal nerves, aiming to lower blood pressure in patients whose hypertension does not respond well to traditional medications. Unlike catheter-based or chemical denervation methods, it emphasizes a non-invasive ultrasound approach and supports its use with multicenter clinical trials (such as the RADIANCE program) to obtain regulatory approvals. The company's goal is to provide a durable, safe method to lower blood pressure and achieve broad adoption of its device in the global healthcare market.

Company size
201-500
Company stage
Debt Financing
Total funding
$40M
Headquarters
Palo Alto, CA
Founded
2009

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