
Clinical Monitoring (all genders)
- Kremsmünster, Oberösterreich
- Unbefristet
- Vollzeit
- Collaborate with a clinical project team to establish project objectives and timelines for IVD/MD trials
- Conduct of IVD and MD studies in accordance with the protocol, standard operating procedures, ISO 14155 & GCP, Regulation (EU) 2017/745 (medical devices), Regulation (EU 2017/746 (IVDs) and Medical Devices Act
- Trial sites feasibilities
- Performance of site initiations, on-site monitoring, monitoring GBO-lab, remote monitoring and close-out visits
- Training of study team members in accordance with protocol specific requirements and (local) regulations
- Ensuring the accuracy, validity and completeness of study data
- Support the (international) trials submission to authorities and ethics committees
- Main contact for study teams and liaison between trial sites and sponsor
- Creation of study specific forms
- TMF maintenance
- University degree in biology, medicine, pharmacy or an equivalent combination of education, training and work experience in clinical trials
- At least 2 years of experience as a clinical monitor (CRA) in 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 and a good understanding of GDPR
- Experience of FDA, ISO regulations and CLSI guidelines is an advantage
- Ability to work independently and reliably in a fast-paced and changing environment
- Excellent communication skills in business fluent German and good written and spoken English skills are a must
- Travelling required