Local Contact Person for Pharmacovigilance and Regulatory Affairs

📋 Description

• Prompt and effective communication with MAH and local regulatory authorities as required
• Primary contact person with local regulatory authorities for Regulatory Affairs and
• Provision of local regulatory intelligence screening and expert advice for the responsible region(s)
• Collection and reporting of locally suspected ADRs or ICSRs (FUs, translations)
• Local management / oversight of risk minimization measures related to urgent safety restrictions
• Support with development and implementation of local pharmacovigilance system in compliance with

🎯 Requirements

• Bachelor's Degree in Life Sciences or Chemistry, Nursing or equivalent professional experience
• At least 3 years of pharmacovigilance or safety-related experience in pharmaceutical, CRO, or
• Good understanding of ICH GVP and local pharmacovigilance requirements (training or practical
• Experience in case handling, literature screening, or local PV activities is preferred
• Prior experience in Regulatory Affairs is preferred but not mandatory
• Proficiency in English and additional language knowledge is advantageous

🎁 Benefits

• When you join Ergomed Group, you make a difference by helping to bring safe and effective
• You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance
• We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a
• Quality: we hold ourselves to the standard patients deserve.
• Integrity and trust: we do the right thing, especially when it is hard.
• Drive and passion: we care about the outcome, because someone is waiting on it.