Patient Journey Director – CEE, Russia, Japan

🔥 19 hours ago

🇯🇵 Japan – Remote

⏰ Full Time

🔴 Lead

👔 Director

Where this job comes from

Posted on Sobi - Swedish Orphan Biovitrum AB (publ)'s careers page ↗Sobi - Swedish Orphan Biovitrum AB (publ)'s careers page, not through a job board

First seen by Remote Rocketship 19 hours ago

Still open on Sobi - Swedish Orphan Biovitrum AB (publ)'s site. Checked 2 hours ago.

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Logo of Sobi - Swedish Orphan Biovitrum AB (publ)

Sobi - Swedish Orphan Biovitrum AB (publ)

1001 - 5000 employees

Founded 1991

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Sobi - Swedish Orphan Biovitrum AB (publ) is a global leader in providing innovative treatments for people with rare diseases. Specializing in therapeutic areas such as haematology and immunology, Sobi is committed to improving patient access to medicines for rare and debilitating conditions. With a strong R&D pipeline, the company is actively pursuing new therapies and collaborating globally to transform patient care in areas such as haemophilia and immune thrombocytopenia. Sobi also engages in extensive sustainability and humanitarian aid programs, demonstrating a firm commitment to patient-centric care and societal contributions.

📋 Description

• Own the patient journey agenda for C3G/IC-MPGN and severe hypertriglyceridemia across CEERJ • Define and refine a regional patient journey framework identifying diagnostic difficulties, delays and post-therapy difficulties • Translate patient journey barriers into prioritized, measurable initiatives • Partner with country leaders and field teams to map and clear country-specific barriers and opportunities • Develop concise, prioritized improvement projects with milestones, owners, dependencies and KPIs • Resource and adjust executive plans as conditions change • Report progress to senior leadership, CEERJ Leadership Team and Brand Team forums • Lead Patient Journey projects and matrix teams from kick-off to close-out, including planning, budgeting, delivery and reporting • Integrate Florio, Enfuse, diagnostics and pipeline tools into patient journey frameworks across CEERJ • Ensure stakeholder value, country readiness and compliant platform use; track adoption and escalate barriers • Collect and synthesize insights from healthcare professionals, key opinion leaders, diagnostic initiatives, patient organizations and country teams • Turn insights into recommendations that influence plans and decisions • Maintain current knowledge of C3G/IC-MPGN and severe hypertriglyceridemia science, diagnostic pathways, competitive and customer landscapes, Tier 1 KOLs and patient advocacy groups • Work in an agile manner, adapting priorities as launches, access and evidence evolve • Communicate executive-ready plans clearly to Brand Teams, Leadership Teams and Core Medical Team

🎯 Requirements

• University degree such as M.D., Pharm. D., or PhD, preferably with biological sciences background • Academic, clinical or industry experience in nephrology, cardiology, endocrinology or immunology • Minimum 2 years’ experience in a commercial field role or medical affairs at a local level from a larger country, with recognized success internally and externally • Experience in Patient Access, Community Engagement or Diagnostics is a plus • Strong business acumen and presentation / communication skills across all organizational levels • Multi-stakeholder project management and leadership experience, with ability to deliver on time and within budget • Strong project management skills and proficiency in Microsoft Excel, PowerPoint and other Microsoft Office programmes • Working knowledge of EFPIA regulations and compliance requirements, with demonstrated highest ethical standards • Fluency in written and spoken English • Ability to think innovatively and strategically, plan, manage and prioritize multiple projects independently • Ability to work independently while maintaining a team and corporate approach • Proactive, open-minded, experienced leader able to identify and carry out strategic initiatives with high patient impact • Strong scientific acumen, leadership, project management and scientific communication skills • Frequent regional and international travel, approximately 40% of working time • Availability for external meetings, congresses and internal meetings outside standard hours with advance notice • Valid driver's license may be required depending on local role set-up • Compliance with applicable laws, regulations, industry codes, internal SOPs and Sobi policies

🏖️ Benefits

• Competitive benefits package supporting the health and happiness of staff • Opportunity to work at an international pharmaceutical company • International, collaborative work environment • Exposure to rare disease research, healthcare, industry and academic backgrounds

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