Holistic Doctor helping people to find the root cause of their problem.Also director of the CRO which is monitoring, auditing and managing clinical research. developing new programs and methods for ageing population together with GP and hospital sites around EU.

Was responsible for the medical strategy in Rheumatology, Pulmonology and Neurology. Working together with market access team was preparing new compounds submissions for the reimbursement in Ireland.

Translating scientific and medical information and building relationships between groups of people, such as physicians and industry personnel. Key responsibilities include: establishing and maintaining peer relationships with key opinion leaders (usually clinical/research leaders in specific therapeutic area); developing educational materials and support programs for personnel; maintaining thorough knowledge of literature and data in therapeutic area. Independently managing home-based work with extensive travel.

Monitoring cardiovascular study in Ireland and UK

Monitoring acquired haemophilia study in UK.

Monitoring cardiovascular and endocrine studies in UK and Lithuania.

QA visits with 100% review and reconciliation of the Trial Master Files (TMF) and review of 100% of each study’s Investigator Site files for the study conducted in Lithuania, Latvia, Estonia, Russia and Ukraine.

Ensure correct conduct of trials in compliance to time, within budget and to the highest possible standards; in accordance with protocols, UK regulations, GCP guidelines, company SOPs and other prevailing standards of best practice. To coordinate the extended project team; to develop accurate project plans for assigned sites; carry out risk analysis and generate contingency plans to meet significance risks to project completion; to monitor progress of projects to enable effective and accurate reporting and project control; to carry out trial feasibility; to assist with the file submissions to the RECs and the Competent Authority; to ensure the studies come in on budget; to write/validate the technical and/or administrative documents which are necessary for the trial; to organize the local investigators meetings, when required; to ensure timely initiation of study sites; appropriate follow-up (co-monitoring, reports, recruitment tracking) and close-out (files archived, IMP and trial material collected) of study sites; to train the CRAs to the study specificities and assist with centre allocation and CRA workload review; to communicate with external relations and internal contacts on a professional level.

Responsible for day by day monitoring activities: PSVs, SIVs, MVs, COVs, Ethics submissions

Monitoring and managing clinical study for one country.

Full time NHS Locum Consultant General/Vascular Surgeon with on call 1/5. All conventional general and vascular surgery.

Vilnius University Emergency Hospital as Vilnius University base has over 600 beds for emergency and elective patients for multiple traumas, abdominal surgery, neurosurgery, urology, gynecology, plastic surgery, orthopedics etc. I was full time NHS Permanent Consultant Vascular Surgeon with on call ¼ week. My main duties: emergency and elective operations as vascular surgeon.