MedQIA, WorldCare Clinical, and DARC have merged to form VOIANT.

MedQIA is now VOIANT. Role includes assisting with the coordination, management, and oversight of the various aspects global clinical trials at the direction of the Director of Clinical Operations (DOCO), providing operational leadership of clinical trials to ensure delivery on time, within budget, and of high quality, in compliance with ICH/GCP, Regulatory Authorities regulations/guidelines, and MedQIA SOPs/MOPs, assisting with operational direction of study teams, providing departmental support, assisting with onboarding and training of new personnel, providing guidance and oversight with Start-up and/or Conduct phases of clinical trials.

MedQIA is now VOIANT. MedQIA is a global, contract research organization specializing in Quantitative Image Analysis for Clinical Trials and Radiological Decision Support (RDS) services. As Clinical Trial Manager (CTM), Mariana is responsible for assisting with the coordination, management, and oversight of the various aspects of MedQIAs global clinical trials at the direction of the Director of Clinical Operations. Mariana provides operational leadership of clinical trials to ensure delivery on time, within budget, and of high quality, in compliance with ICH/GCP, Regulatory Authorities regulations/guidelines, and MedQIA SOPs and procedures. Mariana´s responsibilities also include assistance with operational direction of one or more study team(s) as well as serving as project lead, providing departmental support as needed and upon request, assisting with onboarding and training of new personnel, providing guidance and oversight with Start-up and/or Conduct phases of clinical trials, and performing other departmental activities as needed and upon request.As a Project Lead (Americas, EMEA, APAC), Mariana covers functions such as study start-up activities, overall project management, overseeing Regional PM team functions in general, acting as a liaison between MedQIA and sponsors, project billing and reporting, and final close-out and transfer of record actions.As as Regional PM (Americas, EMEA), Mariana handles management of clinical sites involved in trials requiring imaging transfer to MedQIA Core Lab for central analysis and quantitative review. Mariana also acts as primary liaison with sponsor and between imaging facilities and imaging processing Lab to ensure all Subject images required for a clinical trial are submitted accurately and timely.

Observational 10-year study in Multiple Sclerosis (Phase IV) - local country management and monitoring.

Budget & proposal design/analysis, study start-up (logistics and regulatory affairs), site selection, activation and monitoring, study close-out activities, document and study progress management (regulatory and sponsor-related).http://www.eurotrials.com/

Clinical Trial Organization, Monitoring & Management including budget & proposal design/analysis and regulatory follow-up of clinical trials.http://www.stat-research.com/

CRA quality oversight & co-monitoring in ongoing clinical trials.http://beaufortcro.com/

Part-time consulting as CRA involved in monitoring and regulatory areas within clinical reasearch trial enrollment period.

Clinical start-up & monitoring for a CNS study.http://acic-ccta.org/

Clinical start-up & monitoring for a cardiovascular disease study.http://www.corelabpartners.com/

Basic Research (pre-clinical) activities in Embryology (infertility in women with endometriosis).