Oportunidades laborales

CRA office based

DESCRIPTION: Clinical Trials and Observational studies monitorisation ­

• Full study life cycle: start-up to close-out on site monitorisation for phase I to phase IV studies

• Provide regular and accurate study status reports

• eCRF remote review

• Management of you own agenda and travel resources

• Provide support to project development for files generation and finance control

TYPE OF CONTRACT: Full time, 6 months + permanent contract

REMUNERATION: 1.800-2.000 € net (negotiable)

STARTING ON: March-April 2017

REQUIREMENTS ­

• University Degree on Life Science (Biology, Pharmacy...) ­

• 2 or more years experience as a CRA (preferably in oncology) ­

• Knowledge on GCP guidelines and European Regulatory requirements

• Excellent administrative and IT skills ­

• Experience working with eCRFs

• Availability to travel to national and international locations (50-60% time)

PERSONAL REQUIREMENTS:

• Organization and coordination skills

• Excellent communication and interpersonal skills

• Ability to work under pressure and prioritise

• Ability to work independently and respond to changes

• Fluent in Spanish and English

CONTACT US:

Melissa Fernández Pinto: Esta dirección de correo electrónico está siendo protegida contra los robots de spam. Necesita tener JavaScript habilitado para poder verlo.

Phone: (+34) 912 866 807