The calibrated outsourcing of qualified CRA candidates helps our clients achieve greater human resource management flexibility and improve operational effectiveness. Our deep experience ensures that we staff each study with elite, experienced professionals. All of our employees work in strict accordance with ICH GCP guidelines and all applicable regulatory requirements.
CRA Key Responsibilities
- Perform monitoring visits in accordance with the monitoring plan, ICH-GCP and company SOPs
- Build strong relationships with site staff and investigators and conduct regular remote follow-ups with the sites
- Participate in and organise investigator meetings, where required
- Complete study start-up activities where required (EC/IRB submissions, site contract negotiation & management)
Advance Your Program Today
HungaroTrial is ready to help you complete your clinical trial program on time and to the highest standards.
Clinical development / Phase I-IV. services
We provide exceptional study design, management, monitoring, and reporting expertise for our partners to support their confident decisions for successful clinical development. Our network in the medical community of the CEE Region and long-term KOL connections ensure optimal trial site selection and enrolment rates for our Clients.
Medical device trials and Colsultancy
HungaroTrial’s Expert Team is ready to assist medical device companies through all phases of product development by regulatory consultancy and clinical trial services, with special focus on MDD => MDR transition.
Support for COVID-19 research
From the beginning of the pandemic, HungaroTrial has been very active in COVID-19 clinical research. Our colleagues are dedicated to add our clinical development knowledge, medical expertise and research infrastructure to the global efforts to find safe and effective COVID-19 medications.