FREELANCE CLINICAL RESEARCH ASSOCIATES / PROJECT MANAGERS en FreelanceCRA.com

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FREELANCE CLINICAL RESEARCH ASSOCIATES / PROJECT MANAGERS

Fecha de la oferta: 30 Nov.
Empresa que publica esta oferta: FreelanceCRA.com
FreelanceCRA.com is a project bureau consisting of dynamic, presentable and approachable Clinical Research Associates.

In today´s world of tight deadlines and complex regulatory issues, it makes sense to contract a local, experienced and professional CRA on a freelance basis. Our network brings together these professionals making their qualities work for both themselves and the CRO.

The CRO has a large database available with candidates with the right experience. The CRA has a source of continuous projects with the ability to choose a project rather than to search for on
Empresa que ofrece el puesto:International CROs conducting trials in Spain
Número de vacantes: Sin especificar
Provincia/s: A Coruña, Álava, Albacete, Alicante, Almería, Asturias, Ávila, Badajoz, Baleares, Barcelona, Burgos, Cáceres, Cádiz, Cantabria, Castellón, Ceuta, Ciudad Real, Córdoba, Cuenca, Girona, Granada, Guadalajara, Guipúzcoa, Huelva, Huesca, Jaén, La Rioja, Las Palmas, León, Lleida, Lugo, Madrid, Málaga, Melilla, Murcia, Navarra, Orense, Palencia, Pontevedra, Salamanca, Segovia, Sevilla, Soria, Tarragona, Tenerife, Teruel, Toledo, Valencia, Valladolid, Vizcaya, Zamora, Zaragoza

Descripción

Descripción: We are looking for professionals working as an ´autónomos´ and willing to accept projects on this basis.

To perform clinical monitoring activities in compliance with ICH GCP and Regulatory requirements.

ESSENTIAL TWO YEARS EXPERIENCE in Phase I-IV, epidemiology, observational or postmarketing safety studies.
Tipo de contrato: For the duration of the selected study
Remuneración anual: Depending on duration of the study and contract.
Ventajas sociales o económicas: -Travel, meals and accomodation to and from site will be reimbursed, as will general office costs.
-Excellent pay either per hour or per pre-set budget
-Depending on the size of the projects you can take on several projects part-time.
-You will be in control of your own time-management.
Observaciones: To work autonomously as a freelance CRA you need a certain amount of self-discipline, responsibility and drive.

A personal interview with a representative of FreelanceCRA.com and later with the Sponsor of the selected study is standard procedure.

Requisitos

Requisitos: -Life science, Pharmacy, Biology or Medicine degree.
-Clinical Research Monitoring Masters/course or equivalent experience level.
-Excellent communication skills.
-Representative personality.
-Fluent English and Spanish.
-Computer and software knowle
Nivel de estudios mínimo requerido: Licenciado
Idiomas requeridos: Inglés nivel Alto.
Experiencia profesional mínima requerida: 2 años
Disponibilidad para viajar requerida: El 40% del tiempo laboral

Comparte esta oferta:

Esta oferta ha recibido más de 150 inscripciones.