Senior Clinical Research Associate (oncology) in Czech Republic (m/f/d)

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 client, international pharmaceutical company, we are currently looking for Senior CRAs (at least 3 years’ experience in Clinical Monitoring activities) with current experience with clinical studies on modern oncology therapy. You can expect up to 50% 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 mostly home based (expect to visit the office once per 2 weeks).

Core responsibilities:

• Performing initiation visits, regular monitoring visits and close-out activities.
• 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.
• Working on oncology studies with modern therapy

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.
• Current experience with oncology trials (modern therapy)
• The ability to work with modern software.
• Passionate to provide value to our customers and to learn continuously.

We will be happy to give you more information during a personal meeting or remotely via Teams. By providing your personal data in the materials sent to our company, you consent to their processing and storage in the database in order to obtain employment or business opportunity for you. At the same time, you hereby confirm that the personal information contained in the submitted materials is true and complete.