Manager, Global Scientific Affairs

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Sobi - Swedish Orphan Biovitrum AB (publ)

WebsiteLinkedInAll Job Openings

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

• Support the development and execution of scientific communications and medical activities for assigned assets • Work closely with the Global Scientific Affairs and Medical Affairs leads to ensure high-quality delivery of congress materials, medical education and training initiatives • Focus on operational execution, project coordination, and content support, ensuring timely and compliant implementation of scientific strategies • Assist in drafting, reviewing, and formatting scientific materials • Maintain trackers and ensure milestone adherence • Support development and rollout of internal and external training materials • Coordinate logistics for training activities (content, speakers, timelines) • Track deliverables and ensure alignment across stakeholders • Maintain project plans, trackers, and communication timelines

🎯 Requirements

• Advanced degree (PhD, PharmD) or MSc in life sciences (PhD preferred but can be flexible depending on seniority) • 2–5 years’ experience in Medical Affairs, Scientific Communications, or pharma/biotech • Experience in Cardiometabolic disorders is preferred • Collaborative team player with interpersonal skills, able to work effectively in a team setting and interact respectfully with people of different cultural, seniority and functional backgrounds • Experience in working and collaborating with Market Access, Medical Affairs, Clinical, Legal, Regulatory and Compliance • Role model with the highest scientific and ethical standards, working in accordance with applicable rules and regulations • Outstanding communication skills, both written and oral • Strategic thinking, Prioritisation and time management skills and strong sense of accountability • Proficiency in Microsoft Windows, Word, Excel, and PowerPoint required • Fluency in English, other European languages a bonus

🏖️ Benefits

• Competitive compensation for your work • Emphasis on work/life balance • Collaborative and team-oriented environment • Opportunities for professional growth • Diversity and Inclusion • Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments