Founded in 1997 by Dr Miroslav Reljanovic, Ergomed Plc is dedicated to the development of new drugs to save or improve lives. Operating with a global footprint in over 55 countries, Ergomed has the expertise to manage even the most challenging clinical trials.  Ergomed provides services to over 100 clients in a range of therapy areas but excels in the provision of services for  complex trials in Rare Diseases, Oncology and Neuroscience.

• Training, consultation and support of Study nurses on clinical studies
• Providing non-operational site support to ensure progress of clinical study and to ensure that it is conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and the applicable regulatory requirement(s)
• Notifying Study Monitor / Team on any site issues that are detected in contact with the clinical center and are relevant for them
• Establishing and maintaining relationships with Study nurses and Investigators to optimize performance of clinical study

• Experience as a Clinical site manager, Study nurse or study site coordinator
• Bachelor or Master of Science degree or equivalent
• Proficient English both verbal and written
• Excellent organisation skills with attention to detail
• Excellent interpersonal and communication skills
• Good IT skills (MS Word, Excel, Internet tools)
• Valid work permit for Ukraine 

Our Site Management model is an integrated part of our approach to the management of clinical trials.

Through a network of Site Coordinators serving sites across the globe, this enables us to  offer higher ‘patient-per-site’ ratios in comparison to other CROs. Our team provides continuous and ongoing site support that allows us to achieve enhanced patient recruitment rates whilst maintaining high quality data. Early and meticulous site evaluation in the feasibility process is critical in ensuring accelerated recruitment.

Our unique Site Management Support Solution allows us to offer:

• Faster recruitment
• More patients per site
• Enhanced data quality
• More timely data entry
• Fewer data queries
• Better compliance to GCP