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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

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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.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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