Study Success Director, CEE

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Iterative Health

WebsiteLinkedInAll Job Openings

51 - 200 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Iterative Health is a company focusing on revolutionizing gastrointestinal (GI) care through advances in artificial intelligence and machine learning. They aim to optimize clinical trials and empower physicians with AI tools, particularly for colorectal cancer screening and surveillance. Their mission is to bring precision GI care worldwide by developing a complete ecosystem using cutting-edge technology. Iterative Health combines services and technology to enhance clinical research practices and has been recognized in the field of gastroenterology for its pioneering work and collaboration with leading scientists.

📋 Description

• Serve as the primary Iterative Health point of contact for sponsors and local affiliates, as well as CRO country teams across CEE — owning the relationship and ensuring consistent, high-quality engagement throughout the study lifecycle. • Work closely with European leadership to build and maintain trusted relationships with key regional decision-makers at sponsor and CRO organizations, positioning IH as the partner of choice for new and ongoing studies. • Ensure study kickoffs are well-structured, clearly documented, and set expectations from day one. • Track and report site performance, risks, and follow-up actions accurately, addressing them through regular alignment cadences with sponsors and CROs. • Drive regional network growth by cultivating IH's presence and reputation with existing sponsors and CROs across CEE. • Improve sponsor satisfaction, study retention, and IH's share of new studies within existing sponsor relationships over time. • Build and execute, together with European leadership, a comprehensive stakeholder map and engagement plan for each active and pipeline sponsor and CRO across the region. • Ensure coverage of all key stakeholder types — medical, operational, regulatory, and procurement — with a clear engagement cadence and documented relationship history. • Lead the development of study-specific kickoff materials, RACIs, and communication frameworks that set clear expectations between IH, sponsor, CRO, and site teams from day one. • Facilitate sponsor and CRO kickoff meetings, ensuring IH's role, responsibilities, and value are clearly communicated at the outset of each study. • Educate sponsors early on IH's operating model, site capabilities, and network standards to set the right expectations and reduce misalignment during execution. • Partner across teams to build and maintain an evidence-based service narrative, translating site performance, activation timelines, and execution track record into materials that build sponsor and CRO confidence. • Understand regional sponsor and CRO needs and help translate them into concrete services IH can offer going forward. • Support business development by equipping sponsors with credible, current evidence of IH's network performance, site quality, and delivery track record. • Respond to sponsor and CRO questions about IH's capabilities with accurate, up-to-date regional operational insight. • Own weekly and ad-hoc alignment calls with sponsor and affiliate teams, reporting on site performance, activation status, enrollment progress, risks, and follow-up actions. • Maintain and present clear, accurate performance dashboards and status updates that enable sponsors to make timely decisions. • Escalate site-level risks and sponsor concerns to internal stakeholders early, driving resolution before they affect timelines or relationships. • Perform other tasks as assigned.

🎯 Requirements

• 8+ years of experience in clinical trial operations, sponsor-facing roles, or study management within pharma, biotech, a CRO, or a site network organization. • Proven track record of building and managing sponsor or CRO relationships in an operational capacity. • Deep understanding of clinical trial processes, site operations, and the sponsor-CRO-site dynamic across Central/Eastern Europe. • Experience leading study kickoffs and managing cross-functional stakeholder communication across complex, multi-country studies. • Excellent communication and presentation skills; comfortable engaging senior stakeholders at sponsor and CRO organizations. • Strong organizational skills with the ability to manage multiple sponsor relationships and studies simultaneously. • Ability to independently develop clear and structured presentations, RACI-charts and process flows. • Fluency in English and Polish required; Additional CEE languages strongly preferred. • Willingness to travel approximately 20% across the region for sponsor meetings and kickoff events.

🏖️ Benefits

• Private medical coverage • Life insurance • Retirement benefits • Paid time off