This will be your future job
- In your new role, you will independently lead all activities consisting of assessment, planning, conceptual realization and implementation, as well as review, maintenance and decommissioning of study-specific IRT concepts
- You act independently as an IRT representative in cross-organizational and cross-functional study and project teams and have deep expertise in the technical implementation of IRT concepts and clinical study design related to compliance and drug safety
- You will also contribute to the continuous development of IRT concepts by bringing in new approaches and solutions to keep systems state of the art
- You will ensure that all work is performed with patient safety in mind and in compliance with GMP and GCP as well as US, EU and other international guidelines
What awaits you at FERCHAU
- A wide range of training courses
- Free parking within walking distance of the office
- A real team spirit and passion for what we do
Impress us with your qualifications
- Master's Degree in Natural Sciences and some experiences in a related scientific discipline or Bachelor's Degree with long term experience in a related field
- Experience in the IRT field, knowledge of the technical aspects and functions of an IRT system
- Good understanding of the regulatory and GMP/GCP is desirable and how to apply these to function is advantageous
- Good understanding of global investigational drug activities, as well as general clinical trial execution and design
- Excellent communication skills and fluent in written and spoken English
Our team thrives on diversity. Experts who would like to bring their different strengths to the table for their common goals. Apply now! Online quoting reference JU50-72273-UL to Mrs. Marlen Kopp. The next level awaits you!
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