CRA II, SCRA, Clinical Research Associate, Monitor Ensayos Clinicos, jobs, empleo, trabajo. Sponsor dedicated. Madrid, Barcelona. Oncology, Cardiology, Diabetes, Respiratory, MS, Neurology.
As an integral part of everything we do, our employees make a difference in the lives of millions of people… and you will too.
If you want to accelerate your CRA career, think long term and the possibilities we can offer you. We are a global leading CRO and have helped the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market.
Explore our CRA II and SCRA jobs and see why Covance is known to promote 2.5 more employees annually than average companies.
We have multiple job opportunities: you could work sponsor dedicated, or for different clients (only 2 max. in parallel), at our special ph I unit, or ph II-II… you chose!
Contact us if you are thinking in adding to your career:
We will help you achieve your goals by continuous training & professional development.
As we have multiple jobs available, we have both, home and office based choices.
What does your career need now? Let us know and explore if our current vacancies are a true career move for you.
SALARY RANGES & BENEFITS
If you want to enquire about the salary range, please contact us to discuss.
Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers. Apply now by clicking the “Apply to job” button.
Don´t have your CV ready, not ready to apply, or have some questions first? Connect me or call me, Carlos Villanueva, to discuss in confidence:
CRA II, SCRA, Clinical Research Associate, Monitor Ensayos Clinicos, jobs, empleo, trabajo. Sponsor dedicated. Madrid, Barcelona. Oncology, Cardiology, Diabetes.
University degree (life science ), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification)
Min. 3 years of independent, on-site monitoring experience, including pre-study, initiation, routine monitoring and closeout visits, according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines- oncology experience highly preferred.
Thorough knowledge of ICH Guidelines and GCP, a basic understanding of regulatory requirements and thorough knowledge of monitoring procedures
Full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
Fluent in Spanish and English