Phlebotomist​/Clinical Research Assistant

Want to join a fast-paced, innovative company that is transforming the future of blood testing? Truvian is a healthcare technology company operating at the intersection of diagnostics and consumer technology. We have developed an automated benchtop diagnostic platform that delivers laboratory-quality results in minutes across a broad range of health tests. Our proprietary, FDA-cleared technology is designed to make blood testing more accessible, convenient, and affordable by providing comprehensive results from a single small blood sample in minutes throughout a broad range of locations.

We are continuing to advance our technology’s capabilities to further redefine point-of-care testing and bring high-quality healthcare closer to where patients need it most. 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!

Truvian is looking for an experienced Phlebotomist / Clinical Research Assistant to support to support on‑site blood collection and clinical study execution at Truvian Headquarters. This is a full time, 3 month, temp to hire hourly position. Position is required to be ONSITE. The primary responsibility of this role is to serve as the primary phlebotomist for participant visits, providing skilled venipuncture and capillary collection, a high‑quality participant experience, and accurate specimen collection documentation.

Secondarily, you will work closely with the Clinical Research Coordinator (CRC) and support delegated Clinical Research Coordinator responsibilities, including participant scheduling, visit preparation, study documentation, data entry, and maintenance of study logs. You will also occasionally provide laboratory support, including specimen preparation, processing, handling, and testing activities performed within documented training and authorization. You will collaborate with the Clinical Development Team and internal stakeholders, including R&D, Regulatory, Product Development, Quality, and other cross‑functional partners, to support studies conducted in accordance with the protocol, Good Clinical Practice (GCP), and applicable requirements.

If you want to deepen your knowledge of clinical studies, while working alongside experienced mentors—this role is for you. This role will report to the Clinical Studies Director.

Location:

San Diego, CA (Onsite). This role requires regular onsite work. We welcome applications from qualified candidates; however, relocation assistance is not provided for this position. Candidates should be located within commuting distance of the office.

Candidates must be authorized to work in the United States on a full‑time basis. Truvian does not currently provide visa sponsorship or support employment‑based immigration petitions for this role.

• You will have a hands‑on, participant‑facing role supporting clinical studies at Truvian to generate data that substantiate the performance of Truvian's breakthrough blood testing technology.
• You’ll work with a rock‑star team of people who are passionate about the work they do and our ability to disrupt healthcare with our innovative products.
• You’ll be part of a team responsible for the company’s growth and product launch.
• You’ll thrive in a fast‑paced, dynamic environment where you can implement…