What are the responsibilities and job description for the Clinical Research Specialist position at Greiner Bio-One Americas?
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Responsibility
Job Requirements
Responsibility
- Monitoring of external and internal clinical performance evaluations and internal clinical trials (development studies, post-marketing complaints/observations)
- Preparation of relevant documents for clinical trials according to project requirments and internal processes
- "Preparation of study documents (e.g. templates/protocols)
- "Review of study documents (e.g. templates/protocols)
- Performance of site initiations, on-site monitoring, monitoring GBO-lab, remote monitoring and close-out visits
- Communication with investigators, opinion leaders, consultants, CRO, suppliers
- Filing of documents, TMF maintainance
- Training of study team members in accordance with protocol specific requirements and (local) regulations
- Support the (international) trials submission to authorities and ethics committees
- Ensuring the accuracy, validity and completeness of study data
- Trial sites feasibilities
Job Requirements
- 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 research associate/ clinical monitor in a CRO/medical device or pharmaceutical company
- Good knowledge of current industry practices related to the conduct of clinical trials (ICH-GCP, ISO14155, ISO 20916)
- Good knowledge of MDR and IVDR, as well as good understanding of GDPR
- Experience with FDA, ISO regulations and CLSI guidelines an advantage
- Ability to work independently and reliably in a fast-paced and changing environment
- Excellent communication skills are a must
- Travelling required
- Driving license