Research Assistant
Listed on 2026-01-10
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Healthcare
Clinical Research -
Research/Development
Clinical Research, Research Assistant/Associate
Overview
Circuit Clinical® is on a mission to transform how people find, choose, and participate in clinical research. We are challenging the historical clinical trial methodologies through our work focused on improving access and inclusion in community-based healthcare and through our services that unburden the patients and principal investigators participating in research.
We seek a Research Assistant to join our Team!
As an emerging startup in Buffalo, where New York state fosters rapid and robust growth within the startup community, Circuit Clinical was ranked 20th nationally for Best Workplaces for Innovators by Fast Company® and was named an Inc. Magazine® Best Workplaces 2021. Circuit’s accolades continued beyond the early years as a research industry watchlist company, including winning SCOPE’s Participant Engagement Award in 2022 while continuing to receive national recognition as Fast Company’s World Changing Ideas™ Award 2022.
Over the past year, Circuit has remained committed to breaking the norms that have challenged research participation and continues to extend reach within the research industry, having expanded client relationships with multiple pharmaceutical companies and contract research organizations. And we are not done yet. Our growth knows no bounds as we extended our community-based research into the Midwest during 2023 while growing our remote research capabilities across all 50 US states.
Our award-winning culture is grounded in our values, the heart of the Circuit ethos. We focus on building an incredible, hard-charging Team and providing them the opportunity to do the best work of their careers. In short, we’re motivated to take on the most challenging problems in developing new medicines – this is work that matters to us and those we serve, the patients.
We must recruit the industry’s most dynamic, mission-driven, empathetic, and passionate leaders to accomplish our mission. That’s where you come in!
What We OfferSuppose you’ve been looking for a chance to work with a unique, highly motivated Team and to have a direct impact in building a transformative clinical trials company every day. In that case, that is precisely what we’re offering. We provide competitive benefits and an environment focused on helping you grow personally and professionally.
What You Will Bring to Our TeamAs our Research Assistant you will be responsible for assisting the Research Coordinators by facilitating study protocol visits. You will report to the Lead Research Coordinator and work in collaboration with the entire Clinical Operations team.
How Will You Do ThisAs our Research Assistant
, you are responsible for clinical assessments and phlebotomy, document preparation and reporting, as well as patient recruitment efforts, as well as the implementation of activities associated with research study protocols being conducted in accordance with departmental policy, institutional policy, sponsor requirements, and FDA regulations.
Specific responsibilities include:
- Conduction of study procedures as directed by Research Coordinator, this includes but is not limited to taking vital signs, performing ECGs, and phlebotomy
- Collection, processing, storage, and shipment of laboratory specimens
- Generation and maintenance of laboratory logs
- Inspection and coordination of clinical equipment calibration with qualified vendors
- Management of clinical supply and kit inventory for assigned studies
- Preparation for study procedures including gathering source and essential documents, preparing lab kits and acquiring dry ice
- Documentation of visit data to electronic data capture system (EDC), ensuring entries are accurate, verifiable, and timely. Daily maintenance of system queries
- Assisting in recruitment efforts, contacting and identifying potentially eligible participants to screen.
- Patient recruitment calls as needed
- Additional duties as assigned
- High School degree or higher preferred
- Clinical laboratory and/or phlebotomy experience preferred.
- Proficient in the use of EMR systems preferred.
- Computer literacy including Microsoft office (Word, Excel), Google suite, and CTMS software a plus preferred.
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