Clinical Research Associate (CRA) (m/f/d) in Prague

We love what we do and our business is growing continuously.
Due to the continuous growth we always need good people in different operational working areas of our company. However, our aim is to be the best CRO proving the best services to our clients.
For this reason we only need the best people.

GCP-Service International s.r.o. offers clinical research services throughout Europe using the latest modern technologies. We provide clients with highly professional services based on long-term cooperation, trust and personalized services for either pharmaceutical companies or manufacturers of medical devices.

For our Prague office we are currently looking for Clinical Research Associate with enthusiasm and with at least 1,5 years’ experience in Clinical Monitoring activities. You can expect up to 40% travel work time throughout Czech Republic. The salary will depend on your experience and performance. This gives us the chance to pay good people better compared to our competitors. Position is preferably office based but can be also partially (fully) home based especially during COVID-19 times.

Core responsibilities:

• Working for different internal GCPS projects – medical devices, IMPs, PMCFs
• Performing initiation visits, regular monitoring visits and close-out activities.
• Cooperation with Project Manager on EC and RA submissions
• All monitoring activities to assess the progress of clinical studies at assigned investigative sites to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

Qualifications needed:

• Master´s / Bachelor’s degree in science/health care field or nursing degree or equivalent combined education and experience.
• Fluent in Czech and English, both written and spoken
• Understanding of SOPs, ICH/GCP Guidelines and the national laws and regulations.
• Demonstrates ability to prioritize and manage time for the preparation, completion and follow up of monitoring tasks.
• On-site experience with most types of visits; PSV, SIV, MV, RMV, COV.
• The ability to work with modern software.
• Passionate to provide value to our customers and to learn continuously.