Our client is a global leader in the field of professional services, with a strong focus on digital transformation, technology innovation, and life sciences. The company operates in over 35 countries and works with some of the largest pharmaceutical and healthcare organizations worldwide.
Main responsibilities:
- Review, process, and quality-check adverse event reports to ensure accuracy and compliance.
- Translate source documents (German/English) and update safety databases.
- Perform case triage, duplicate checks, and data entry into safety systems.
- Anonymize/redact documents and generate follow-up letters when required.
- Support audits, inspections, and adherence to regulatory guidelines (ICH, SOPs).
- Handle queries, ensure data completeness, and provide feedback to improve quality.
- Collaborate with colleagues and contribute to training and mentorship activities.
Required skills:
- Degree in Life Sciences, Pharmacy, Medicine, or related fields.
- At least 1 year of experience in pharmacovigilance, drug safety, clinical research, or healthcare.
- Fluency in German and English (minimum B2 level).
- Strong attention to detail and ability to work with complex data in a structured way.
Advantages:
-
What our partner can offer to you:
- Full remote work with 1 office presence/month
- Competitive salary and cafeteria benefits
- Discounted All You Can Move SportPass,
- Medical insurance,
- Risk and accident coverage
- Language course reimbursement
- Inspiring and multicultural work environment
- Training, certifications, and career development opportunities
- Exciting company events, team-building activities
- Annual bonus for top performers, salary review, and recognition programs