CRA II - Oncology - Sponsor Dedicated (top 5 pharma)
- Employer
- Labcorp
- Location
- Madrid (Provincia), Comunidad de Madrid (ES)
- Salary
- Competitive Package
- Start date
- 25 Jul 2019
- Closing date
- 24 Aug 2019
View more
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Discover new opportunities to grow your career as a Covance FSP CRA
CRA II position available to work directly with a top 5 BioPharmaceutical company. As an experienced CRA you’ll be involved in initiation, routine & close out visits concentrating on sites in Spain. Successful candidates will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE!
Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit’ targets
Join a stable team of CRAs across Spain and benefit from outstanding training and development, both initially and throughout your career
Join a company where people tend to stay for 6-10 years rather than 1-3!
Join a genuinely friendly and supportive company where they allow individuals to take ownership of their own performance.
Duty Highlights
As a CRA you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.
Responsibilities Include
All aspects of site management as prescribed in the project plans
Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.
Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems
Other Information
This CRA II role is a full time & permanent position employed through Covance
- University or college degree, or certification in related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
- Valid Driver’s License B
- Thorough knowledge of CGP-ICH and basic understanding of the regulatory requirement
- At least 2 years of independent monitoring experience.
- Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- Previous experience in Phases II and III trials
- Previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) in Italy.
- Fluency in English.
- Oncology is required
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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