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

Yd-895 - Fisioterapeuta Tardes Por Encima De Convenio. El Cañaveral (Madrid)

Resumen del puesto:Buscamos fisioterapeuta para unirse a nuestra clínica de fisioterapia ubicada en El Cañaveral (Madrid). Fisioterapia Escalante.Inicio el 1...


Fisioterapia Escalante - Madrid

Publicado 14 days ago

Óptico-Optometrista Cc Plaza Nueva, Madrid - Media Riv-546

¿Eres Óptico y buscas un nuevo reto profesional en Leganés? ¿Buscas seguir formándote y desarrollándote como optometrista?¿Cómo será tu día en Alain Afflelou...


Alain Afflelou - Madrid

Publicado 14 days ago

Medical Manager, Rare Disease - Iberia

.Job DescriptionAbout This RoleThe Medical Manager, Rare Disease - Iberia is responsible for leading medical strategy and activities for the Biogen SMA (Spin...


Biogen Idec - Madrid

Publicado 14 days ago

Grp-865 | Logopeda

En nuestro Centro de Atención Integral a la Infancia abordamos todos aquellos problemas que se presentan en la población infanto-juvenil a través del tratami...


Centro Ágora® - Madrid

Publicado 14 days ago

Clinical Project Coordinator - Entry Level

Detalles de la oferta

.Due to continuous business growth and a strong study pipeline, we are looking for Project Coordinators to join our successful and growing Spanish team and engage in clinical trial management on a day to day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company's success. This position will provide extensive training and is suitable for recent graduates; internship, industrial placement, Clinical Trials experience is also beneficial.ResponsibilitiesWork closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; Maintain and track study supply inventory for study sites and coordinate shipping efforts of study materials; Compile and maintain project-specific status reports within the Clinical Trial Management System (CTMS); Interact with the internal project team, Sponsor, study sites, and third-party vendors; Ownership of the Trial Master File; Create and maintainproject timelines and enrolment projections; Coordinate project meetings and produce quality minutes.QualificationsMasters' Degree in Life Sciences; Excellent oral and written English Language communication skills; Knowledge of Microsoft Office programs; Experience in a health sciences or business setting preferred; Excellent organisational and prioritisation skills; Ability to work collaboratively on projects with others; Strong attention todetail.We ask that you please submit your CV in English.Medpace OverviewMedpace is a full-service clinical contract research organisation (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future


Salario Nominal: A convenir

Fuente: Jobtome_Ppc

Requisitos

Built at: 2024-11-11T01:37:23.297Z