Pharmacovigilance Coordinator

Pharmacovigilance Coordinator

Ferring Pharmaceuticals

Copenhagen, Denmark

The job – Focus on quality and process

Your overall focus is to deliver high quality case handling for internal stakeholders and authorities in order to comply with local legislation and conventions. More specifically, you will process adverse events reported worldwide on Ferring’s marketed products and development products in clinical trials. Your primary tasks will include:

• Case intake, data entry and coding of adverse events;
• Training and presentations to colleagues within the department and cross-organizationally;
• Participation in audits and inspections;
• Ongoing guidance and support to colleagues;
• Cross-functional activities in matrix teams.

Qualifications - Experience within Pharmacovigilance

We are looking for a profile that already has experience within the pharmacovigilance case handling area. You have a relevant educational background e.g. Master in pharmaceuticals /science, nurse or similar and are fluent in English both written and oral. As you play a key role in upholding our license to operate, you must have a genuine quality mindset backed by the overview and attention to detail, to ensure high quality data entry.

Additionally, it would be considered an advantage if you also have:

• Years of experience within Pharmacovigilance;
• Extensive experience within safety data handling;
• Experience with LEAN or similar is an advantage;
• Experience with handling deviation or similar Quality System understanding.

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Denmark      Clinical Research      Pharmacovigilance and Medical Information      Ferring Pharmaceuticals