Job Overview :
Wide varietyof CRA II & SCRA jobs in Spain : client dedicated or working in-house on Covance studies
Generous Welcome Bonus if you join us now!
Top 5 pharmaceutical clients
Therapeutic experience required : Oncology
WHERE WILL YOUR CURIOSITY TAKE YOU?
Covance Spain offers unique job opportunities to gain exposure across the broadest oncology / Infectious diseases clinical trial portfolios.
Whether your ambition is to work sponsor dedicated or with different clients, we have the right job for you.
Covance Spain are living an unprecedented growth so we are in the position of offering a wide variety of Clinical Research Associate II (CRA II) and Senior Clinical Research (SCRA) job opportunities :
WHAT MAKE THESE JOBS SPECIAL?
No matter which team you chose you will experience :
Our employees make a difference in the lives of millions of people and you will too.
Join us and see why LabCorp / Covance have been named for the second consecutive year to FORTUNE s 2019 List of World s Most Admired Companies and more than 90% of the top 20 global pharmaceutical companies are repeat customers.
We can offer you not only a job, but a stable, long-term international career.
THE CRA JOB : In terms of location :
In terms of location :
We need you to be based in Madrid / Barcelona, and we can offer you to participate in a wide variety of :
In terms os skills :
Education / Qualifications :
University degree, life science.
Extensive knowledge of :
Extensive clinical monitoring experience in Spain is needed, minimum 2 years monitoring studies in Oncology / Infectious diseases / HIV with proven track record of pre-
study, initiation, routine monitoring and closeout visits.
Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
Ability to resolve project-related problems and prioritize workload for self and team
Advanced site monitoring & study site management skills
Ability to work with minimal supervision
Good planning and organization skills
Good computer skills with good working knowledge of a range of computer packages