Manager, Global Scientific Affairs

🔥 1 minute ago

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 • Ensure timely and compliant implementation of scientific strategies • Assist in drafting, reviewing, and formatting scientific materials • Maintain trackers and ensure milestone adherence • Coordinate congress deliverables • Liaise with internal stakeholders and agencies for content development • Ensure alignment of materials with scientific and compliance requirement • Support development and rollout of internal and external training materials • Coordinate logistics for training activities (content, speakers, timelines) • Maintain training materials repository and updates • Act as a key operational interface with Medical Affairs, Regulatory & Compliance, Clinical and Market Access, Affiliate medical teams • Track deliverables and ensure alignment across stakeholders • Prepare internal updates, slide decks, and reporting materials • Maintain project plans, trackers, and communication timelines • Identify risks or delays and proactively escalate • Support implementation of digital/multichannel initiatives • Ensure documentation is compliant and audit-ready • Conduct literature searches and summarize key scientific insights • Monitor external developments relevant to assigned assets • Support preparation of internal scientific briefings • Contribute to innovative digital/multichannel approaches for the dissemination of medical materials • Stay abreast of internal and external developments relevant to the assigned assets

🎯 Requirements

• Advanced degree (PhD, PharmD) or MSc in life sciences • 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