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Sr. Clinical Research Specialist

Iterativehealth

Cambridge, MA or New York, NY (Cambridge, New York) permanent

Posted: February 13, 2026

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Quick Summary

We are seeking a Sr. Clinical Research Specialist to join our team in Cambridge, MA or New York, NY. The ideal candidate will have experience in clinical research and a strong background in gastrointestinal (GI) and hepatology. The successful candidate will be responsible for driving the success and growth of our partner sites by empowering them with tech-enabled services.

Job Description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and hepatology novel therapies. Our focus is on driving the success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

At Iterative Health, we are pioneering the application of powerful, proprietary artificial intelligence tools to the practice of cardiology and drug development. We’ve set out to drastically improve clinical decision-making while meaningfully improving patient lives through better diagnosis, disease management, and treatment, leading to better health outcomes.

As the Senior Clinical Research Specialist I, you will report to the Head of Cardiology and Growth and work closely with the Director of Clinical Research (Cardiology), and work to integrate Iterative Health (IH) services and AI solutions at cardiology-based, clinical research sites throughout the US. This external-facing role will require strong communication, customer engagement and deep expertise in clinical research, in addition to a strong strategic skill set. You’ll work directly with your portfolio of sites by using our standard methodology to assess their current state. You’ll then work with your assigned sites to deliver customized training and day-to-day support that encourages research best practices, drives the adoption of IH services and products, and ensures our sites achieve their research goals.

Key Responsibilities:

• Demonstrate advanced knowledge of clinical research processes and tools, such as CTMS, pre-screening, and/or feasibility, and enhance these processes and outputs to effectively support our sites or internal teams.

• Serve as a subject matter expert on clinical research workflows, in line with specific requirements of each protocol, optimized with Iterative Health (IH) services and AI solutions

• Manage customer relationships with a high degree of professionalism and expertise ensuring timely responses, escalations of site issues, and building trust needed to help sites achieve IH goals

• Leverage IH solutions and services to help build best practice research sites, accelerate clinical trials, and build capacity at IH sites to execute high-quality clinical trials.

• Deliver customized training for different clinical research user groups and devise process maps/workflows, tools, and techniques to help sites incorporate IH services

• Travel to customer sites to support study site activation, drive patient screening, and standby support for randomization activities

• Collect, analyze, and communicate the voice of IH customer successes, concerns, and product adoption issues/competency gaps and collaborate with IH cross-functional teams to design and deliver solutions

• Monitor personal and site goals and KPIs and flag areas where additional support or assistance is needed

Required skills:

• BS/BA or higher degree.

• Minimum 4 years of clinical research coordinator experience.

• At least 8 years of experience with phase 2-4 pharma-sponsored clinical trials, including study start-up, CDA, feasibility, regulatory/standard operating procedures, study protocols, and regulations governing clinical research

• Experience coordinating, evaluating, and following patients’ participation through clinical trials.

• Fluent in the use of Microsoft Office/Google Apps products.

• Ability to navigate ambiguity and willingness to be flexible/adapt to changing work environments.

• Desire to work with new tools and technology.

• Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately. ● Willingness to travel to customer sites (~30%)

Preferred skills:

• 5+ years as a Clinical Research Coordinator (CRC) working with cardiology trials or equivalent experience.

• General understanding of the evaluation and diagnosis of common cardiac disorders and diseases.

• Experience with CTMS systems - preferably RealTime, Clinical Conductor, or CRIO

New York pay range
$85,000—$105,000 USD

At Iterative Health, we’re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

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