Global Safety Scientist
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| Company Name | Sobi – Swedish Orphan Biovitrum AB (publ) |
| Company Type | Private |
| Job Type | Full-Time |
| Salary Range | Market Competitive |
| Location | Stockholm, Stockholm County, Sweden |
| Qualifications | None / No Formal Education |
| Experience | 5 Year+ |
Job Overview
Sobi is seeking a Global Safety Scientist to join their team in Stockholm, Sweden. This role is crucial for ensuring the safety of breakthrough innovations in rare diseases, contributing to the company’s mission of transforming everyday life for patients.
Company Overview
Sobi – Swedish Orphan Biovitrum AB (publ) is a global biopharma company dedicated to unlocking the potential of breakthrough innovations and transforming everyday life for people living with rare diseases. With strong roots in Sweden, Sobi has grown into an innovative leader in rare diseases with a global reach, employing approximately 1,900 individuals across various continents. The company’s shares are listed on Nasdaq Stockholm.
Quick Details
- Salary Range: Market Competitive
- Job Type: Full-time
- Qualifications: None / Open to all applicants
- Experience: 5 Year+
Key Responsibilities
- Monitor and evaluate safety data from clinical trials and post-marketing sources globally.
- Contribute to the preparation of aggregate safety reports, ensuring compliance with regulatory requirements.
- Perform signal detection and risk-benefit assessments for Sobi’s product portfolio.
- Collaborate with cross-functional teams, including Clinical Development, Regulatory Affairs, and Medical Affairs.
- Provide expertise and support for safety-related queries from internal and external stakeholders.
- Ensure adherence to global pharmacovigilance regulations and internal Standard Operating Procedures.
Requirements
- Demonstrated experience in pharmacovigilance or drug safety within the pharmaceutical industry.
- Strong understanding of global pharmacovigilance regulations (e.g., GVP, FDA, ICH).
- Excellent analytical skills and ability to interpret complex scientific and medical data.
- Effective communication skills, both written and verbal, for diverse audiences.
- Ability to work independently and collaboratively in a fast-paced, international environment.
- Proficiency in safety databases and electronic document management systems.
Benefits
- Opportunity to work for a global biopharma leader focused on rare diseases.
- Contribute to life-transforming innovations for patients worldwide.
- Collaborative and inclusive international work environment.
- Opportunities for professional development and career growth.
- Competitive compensation and benefits package.
- Engaging work culture with a strong emphasis on scientific excellence.