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CRA II, PARIS

Employer
Labcorp
Location
Rueil-Malmaison, France
Salary
Competitive
Start date
18 Nov 2020
Closing date
18 Dec 2020

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Job Details


COVANCE

With all the uncertainty in the world, your job stability should not be a concern.

Covance have supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. But we are much more than a normal CRO:

  • We are also the world´s biggest Central Lab, generating more clinical trial data than all other central laboratories combined
  • Our Early Phase Solutions have proved to shave off 30 % time from lead candidate to Proof of Concept
  • LabCorp/Covance were the first in receiving FDA approval to perform COVID19 tests using an at-home collection kit.


Join us and see why Covance are uniquely positioned to offer you not only a job, but a stable, long-term international career, and why more than 90% of the top 20 global pharmaceutical companies are repeat customers.

THE JOB

We have opened 2 CRA II jobs in Paris

These jobs would suit CRAs who already have minimum 2 years independent clinical monitoring experience in France with international ph I-III clinical trials, within pharma or CRO environment.

  • Experience monitoring ph I-III clinical trials in oncology is a must for the job
  • Ideal location: Paris , home or office based
  • We need you to be fluent in French & English


IS THIS YOU?

At Covance we trust our CRAs and so we will give you autonomy to organize your work. In turn, we expect you to go beyond the typical CRA role and really be an expert of your protocol and to own your sites .

  • Your focus will be direct site management and we expect you to influence site performance


  • We need your hands-on experience nurturing a collaborative relationship with your sites: how will you make the study relevant for them? How will you efficiently solve their issues and answer their questions about systems, documentation, filing or building audit-ready habits?


APPLY NOW

... so we can tell you about the team support that permeate everything we do, how our managers constantly review study/site allocation to ensure workload balance or why you will not grow a stale career with us because you can choose between therapeutic areas, types of clients, etc.
Education/Qualifications:
University life science degree
Experience:
Clinical monitoring in Oncology studies ph I to III is needed.

Excellent understanding of Serious Adverse Event (SAE) reporting

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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