We are offering a workplace that feels like home at Greiner Bio-One. The position involves clinical project management expertise, including obtaining proposals, managing clinical performance evaluations, and supporting product requirements.
Requirements
- Degree in life sciences or equivalent combination of education, training and work experience in clinical trials
- At least 3 years of experience as a Clinical Project Manager (CPM) or 5-6 years as Clinical Research Associate (CRA) at a CRO/medical device or pharmaceutical company
- Good knowledge of current industry practices related to the conduct of clinical studies (ICH-GCP, ISO 14155, ISO 20916)
- Good knowledge of MDR and IVDR
- Good knowledge of FDA requirements related to IVDs and MDs, ISO regulations and CLSI guidelines
- Good understanding of the GDPR
- Ability to work independently and reliably in managing multiple projects (international) and in a fast-paced and changing environment
- Excellent communication skills
- Excellent presentation and diplomacy skills, with the ability to negotiate and resolve conflicts
Benefits
- Equal opportunities for everyone
- Diversity as our strength
- Inclusive work environment
- Empowering women and increasing female leader representation
