Research Assistant at Circuit Clinical

Secaucus, New Jersey, United States -

Full Time

Start Date

Immediate

Expiry Date

21 May, 26

Salary

27.0

Posted On

20 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Assessments, Phlebotomy, Document Preparation, Reporting, Patient Recruitment, Protocol Visits, Laboratory Specimens, Equipment Calibration, Clinical Supply Management, Data Capture System, EMR Systems, Microsoft Office, Google Suite, CTMS Software

Industry

Research Services

Description

Description 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 Per Diem 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 Offer Suppose 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 Team As 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 This As 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 Your qualifications include: 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. Who You Are We prize 4 traits above all others: Hungry: we like people who are ambitious for themselves AND for our Mission and for each other – will all win together and that takes real drive Happy: we seek pragmatic optimists – pessimism and ironic dispositions, especially in leadership can kill startups – we seek those who know the world can be improved by those who work hard and work smart to change it Humble: not the false “I’m not really anything” kind of modesty – we like swagger! But we prize people who are confident and know they are great, and so is everyone around them, and we act accordingly Smart: there are a LOT of smart people here, but smart is last for a reason. We want the kind of smart people who can collaborate and respect the intelligence of others. Location: This position is an on-site position, based at our site in Secaucus, NJ. Exemption status: Per Diem, non-exempt, working the maximum of 10 hours per week. Physical requirements: the following physical requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions: Regularly required to sit; use hands; reach with hands and arms; talk and hear. Specific vision abilities include close vision Other duties: the duties and responsibilities described are not a comprehensive list and that additional tasks may be assigned to the employee from time to time; or, the scope of the job may change as necessitated by business demands

Responsibilities

The Research Assistant will be responsible for clinical assessments, phlebotomy, document preparation, reporting, and patient recruitment efforts, implementing activities associated with research study protocols. Specific duties include conducting study procedures like vital signs, ECGs, and phlebotomy, managing lab specimens, and documenting visit data into the EDC system.