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Research Site Manager

Iterative Scopes - Providence, RI, United States - In-office

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Iterative Health is a healthcare technology and services company accelerating clinical research across gastrointestinal, hepatology, obesity, and cardiology. The company operates a network of 100+ research sites globally and combines clinical trial expertise with AI to connect sponsors with high-performing research teams. As Research Site Manager, you will be the operational leader of one or more clinical research sites, owning day-to-day execution of clinical trials and managing site performance. This is a hands-on management role requiring both strategic oversight and willingness to contribute as a Clinical Research Coordinator when needed. Key Responsibilities: - Manage site staff (CRCs and RAs), including hiring, onboarding, performance reviews, and development - Drive enrollment performance and ensure studies meet quality, compliance, and efficiency standards - Create and implement standardized clinic workflows that support operational excellence - Oversee study supply inventory and site-level purchasing within cost guidelines - Ensure timely completion of tasks in EMR and CTMS systems - Lead onsite training during study initiation visits and ongoing staff development - Monitor performance metrics and address gaps; escalate systemic barriers to central management - Maintain effective communication with CROs, sponsors, Principal Investigators, and referring physicians - Conduct regular site research meetings to discuss progress and enrollment - Manage third-party vendors and ensure contracts are executed before study activation - Ensure compliance with human subject research regulations and protect participant rights - Attend site selection and initiation visits Required Qualifications: - Bachelor's degree from accredited institution (science disciplines preferred) - Minimum 3 years as a senior Clinical Research Coordinator - Strong written and verbal communication skills - Ability to read, interpret, and apply clinic policies and research protocols - Proficiency in standard office software; EMR and CTMS experience preferred - Highly organized with ability to manage multiple priorities and meet deadlines - Strong problem-solving and decision-making under pressure - Professional interaction with staff, investigators, sponsors, and cross-functional partners - Willingness to travel across facility sites and to company meetings Preferred Qualifications: - GI and hepatology clinical trial experience - Prior site management or team leadership experience in clinical research - Familiarity with Iterative Health tools (CTMS, EMR, Salesforce) - Experience in research site networks or multi-site clinical trials - Knowledge of GCP guidelines and human subject research regulations Iterative Health operates with a collaborative, low-ego team environment emphasizing high ownership, accountability, and continuous learning. The company is mission-driven, focused on improving patient outcomes and building an equitable, inclusive culture.

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