FREELANCE CLINICAL RESEARCH ASSOCIATES / PROJECT MANAGERS | |
| Fecha de la oferta: | 31 Ene. |
|---|---|
| Empresa que publica esta oferta: |
FreelanceCRA.com Ver todas sus ofertas de empleo |
| 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 |
| Localidad del puesto: | Locations all over Spain and Europe |
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. |
| Edad máxima para el puesto: | 65 años. |
| 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 38 inscripciones.
