Lo sentimos, la oferta no está disponible,
pero puedes realizar una nueva búsqueda o explorar ofertas similares:

Analista De Canales Internos Y Contenido

**Despega hacia tu próximo destino**En Avianca sabemos que **¡VAMOS A GANAR! **con personas talentosas, divertidas, que aprendan rápidamente, que se motivan ...


Desde Avianca Ar - Bogotá D. C.

Publicado 12 days ago

Clinical Research Associate

The role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA manager the person ensure...


Bogotá D. C.

Publicado 13 days ago

Encuestador Con Moto

Somos la agencia tecnológicamente más evolucionada de Latinoamérica, que durante más de 25 años hemos desarrollado expertis en Investigación de Mercados, per...


Desde Levantamiento De Servicios De Campo S.A. - Bogotá D. C.

Publicado 8 days ago

Encuestador Con Moto- Indispensable

Somos la agencia tecnológicamente más evolucionada de Latinoamérica, que durante más de 25 años hemos desarrollado expertis en Investigación de Mercados, per...


Desde Levantamiento De Servicios De Campo S.A. - Bogotá D. C.

Publicado 8 days ago

Research Assistant (Part Time - Barranquilla)

Research Assistant (Part Time - Barranquilla)
Empresa:

Iqvia


Detalles de la oferta

Job OverviewPerform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.Essential Functions• Provide clinical research support to investigators and site staff, including• Verify and/or correct research study information on source documents; research queries and variances; and providefeedback to the site data collector.• Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,accuracy, and completeness.• Prepare and maintain research study files. Compile, collate and submit study information within established deadlines.• Collect and submit regulatory/ethics documentation pertaining to the research study.• Maintain the FDA 1572 form for assigned research studies.• Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.• Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.Qualifications• High School Diploma or equivalent High School Diploma Req• Educational equivalent and 2 years' relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Req• Basic knowledge of clinical trials• In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and studyschedules• Basic knowledge of medical terminology• Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word• Excellent interpersonal skills• Ability to pay close attention to detail• Ability to establish and maintain effective working relationships with coworkers, managers and clients• Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies Upon Hire ReqIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at


Fuente: Talent_Ppc

Requisitos

Research Assistant (Part Time - Barranquilla)
Empresa:

Iqvia


Built at: 2024-05-18T02:45:49.401Z