The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH‐GCP, and all applicable regulatory requirements.
As a key member of the clinical operations team you will be at the forefront of clinical trials practice, implementing and monitoring trials, ensuring that sponsor and investigator obligations are met, and overseeing compliance with ICH GCP and FDA or European regulatory requirements. You will be working on a wide spectrum of projects in phase I-IV research at both GP practices and hospitals.
To succeed as a Clinical Research Associate you will have a commercial as well as a clinical focus with a real commitment to client service. Essentially, you will bring a Life Science degree, and relevant industry/CRO experience. Fluency in the host language and English is required.
Together with a competitive salary, we offer a comprehensive range of benefits and an excellent working environment. As we continue to expand, there will be career opportunities on a truly global scale.
PRA International - il y a 23 mois
The story of PRA Health Sciences would naturally talk about how we’ve become one of the world’s largest CROs. It would talk...