
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.
🔥 20 hours ago
Where this job comes from
Posted on Sobi - Swedish Orphan Biovitrum AB (publ)'s careers page ↗, not through a job board
First seen by Remote Rocketship 20 hours ago
Still open on Sobi - Swedish Orphan Biovitrum AB (publ)'s site. Checked 1 hour ago.

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.
• Own the patient journey agenda for C3G/IC-MPGN and sHTG across CEERJ • Define, maintain and refine a regional patient journey framework • Identify diagnostic difficulties, delays and post-therapy difficulties and translate them into measurable initiatives • Partner with countries to map and clear patient journey barriers and opportunities • Work with country leaders and field teams on awareness, testing access, laboratory and biopsy pathways, referrals, expert centres and non-pharmaceutical therapy optimization • Develop prioritized patient journey improvement projects with milestones, owners, dependencies and KPIs • Resource and adjust 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 • Ensure project planning, budgeting, delivery and reporting on time and within budget • Integrate Florio, Enfuse, diagnostics and pipeline tools into patient journey frameworks • Ensure stakeholder value, country readiness and compliant use of medical devices and enabling platforms • Track adoption, escalate barriers and propose solutions • Collect and synthesize insights from HCPs, KOLs, diagnostic initiatives, patient organisations and country teams • Turn patient journey insights into recommendations that change plans and decisions • Maintain current knowledge of C3G/IC-MPGN and sHTG science, diagnostic pathways, competitive and customer landscapes, Tier 1 KOLs and patient advocacy groups • Maintain knowledge of related areas including PNH and haemophilia
• 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 • Recognized success internally and externally • Experience in Patient Access, Community Engagement or Diagnostics is a plus • Strong business acumen and presentation / communication skills • Multi-stakeholder project management and leadership experience • Demonstrated ability to deliver results on time and within budget • Strong project management skills • Proficiency in Microsoft Excel, PowerPoint and other Microsoft Office programmes • Working knowledge of EFPIA regulations and compliance requirements • 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 and experienced leader • Ability to identify and carry out strategic initiatives with high patient impact in launches and life-cycle management • Strong business and 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
• Competitive benefits package supporting employee health and happiness • International biopharmaceutical company environment • Global company culture and opportunities to work with international teams
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