Director, Clinical Data Management & Data Science

ABOUT TRUVIAN Want to work for a fast-paced and disruptive company that is working to revolutionize blood testing?

Truvian is a healthcare company at the intersection of diagnostics and consumer tech.

We are developing an automated, benchtop diagnostic system to provide lab-accurate results in 30 minutes for a comprehensive suite of health tests.

Our proprietary approach, for which we are seeking FDA clearance, is intended to fulfill the promise of delivering accessible and affordable blood testing from one small blood sample, in minutes, in a retail setting or private clinic.

To us, our work at Truvian is more than a job – It’s a mission.  We are a culture dedicated to discovery and empowerment.

We are trailblazers on the path to put health information where it belongs - in the hands of the individual.

We are partners in the belief that talented people, working as a team, can make every day an adventure.

Come join us as we realize our vision to make routine health testing convenient, affordable, and actionable for today’s connected consumers!

JOB SUMMARY Truvian is seeking a strategic and technically adept Director, Clinical Data Management & Data Science build and lead a multidisciplinary team responsible for clinical data strategy, management, analytics, and statistical sciences.

This role is pivotal in ensuring data integrity, regulatory compliance, and operational efficiency across the product lifecycle—from early research through regulatory submission and post-market surveillance.  This position is ONSITE.

The Director will architect and scale Truvian’s clinical data ecosystem — spanning database design, data pipeline integration, clinical data quality, statistical analysis, and data visualization — to support assay validation, regulatory submissions, and real-world evidence generation.

The ideal candidate combines strategic leadership with hands-on technical expertise in biostatistics, clinical data systems, and data science for diagnostics.

This role requires in-depth expertise in the IVD industry, including knowledge of FDA regulations (21 CFR Part 11, Part 820), and a proven ability to lead data initiatives in a regulated environment.

HERE’S WHY YOU WILL LOVE THIS ROLE Unique Growth Opportunity :

• Gain hands-on experience across clinical studies, data analysis, regulatory submissions, and product development.

Data-Driven Innovation :

Fast-Paced Start-Up Culture :

Professional Development :

Meaningful Impact :

You love and thrive in a fast-paced and dynamic environment where you can implement fresh ideas, new processes, and make things happen quickly without a bunch of red tape You’ll have great perks such as :

WHAT YOU WILL BRING Required :

Preferred :