Coordinador administrativo de protocolos de investigación clínica en Nuevo León - Importante empresa del sector farmacéutico Otro

de Importante empresa del sector farmacéutico en Nuevo Leon
Publicado el 19-10-2016 en Salud

Administrar y coordinar proyectos de investigación clínica. Trato con personal médico y pacientes, elaboración de reportes, revisión y envío de información, etc.
You must be reliable, punctual, motivated, looking for work within a research environment and have a flexible attitude to work.
Demonstrated ability to interact with different professional levels of the medical community.
The ability to function independently without minimal or no daily supervision.
Experience working as part of a team.
Self-motivated, tenacious and displays initiative.
Proven organizational skills and the ability to prioritize and manage multiple tasks.
Attention to detail.
Analytical and conceptual thinking skills - is able to critically evaluate and solve problems.
Proficient in various computer applications including spreadsheets, email, word processing software and the web.
Daily Tasks: Study coordinators work directly with study volunteers, providing them safety and protection while collecting and managing the study data. They promote, advertise, and conduct telephone and face-to-face screenings to recruit volunteers. During the study process, they assess volunteer condition and coordinate ongoing clinical/laboratory testing and physical exams. Study coordinators follow up with volunteers after the study and manage a great deal of paperwork, electronic correspondence and data.
Skills/Talents: Strong interpersonal skills, ability to communicate with patients, ability to educate patients, compassion and a desire to help people. Must have strong communication skills, organizational skills, attention to detail and the ability to adapt to change and work with other employees. Word processing and spreadsheet computer skills are essential.

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