Covance

  • Clinical Trial Assistant (CTA) - Sponsor Dedicated

    Job Location(s) IT-Milan
    Job Number
    2018-25992
    Job Category
    Clinical Trial Support
    Position Type
    Full-Time
  • Job Overview

    WHY COVANCE?

     

    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 CTA 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 CTA jobs and see why Covance is known to promote 2.5 more employees annually than average companies.

     

     

    THE JOB

     

    Our sponsor-dedicated team is expanding in Spain. 

    We have Clinical Trial Assistant/ CTA jobs available to work directly with large Pharmaceutical companies in cutting edge areas like Oncology, Cardiology or Diabetes.

    You will provide support to CRAs and CTLs with: essential document collection, Site Initiation Visits, amendments... Your trained-eye will be vital to perform study documents QC review for archiving (paper and eTMF). You will set up and maintain investigator files, personalize contracts for sites. You will also be involved in payments and contracts.

     

     

    Our sponsor dedicated CTA jobs ensure that you will have a VARIED role, not rigidly fragmented in the same repetitive tasks day-after-day, forever …

     

    We take good care of ENRICHING the CTA job content, now AND in the future: on-site CRA support, international assignments, responsibilities in safety, quality, IMP…

     

     

    What does your career need now? Let us know and explore if our current jobs are a true career move for you.

     

     

    REQUIREMENTS

     

    You are a CTA working in Madrid (By the way: initially, you will work office based, and once you know the systems and processes you could work some days from home on a weekly basis if you choose.)

     

    We need you to bring min 1.5 yrs experience working at a CRO or Sponsor, with background supporting CRAs in international ph I-IV clinical trials. This is an international environment, so you could use your English skills during meetings or translating key documents.

     

    Your aptitude for handling and proofreading numerical data and your spreadsheet software competency will be essential to avoid delays and issues during the course of the project.

     

    Diploma – Secondary Education or equivalent.



    We will help you achieve your goals by continuous training & professional development

    Education / Qualifications

    *

    Experience

    *

    Options

    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed

    Tell Us About Yourself

    Not ready to apply? Connect with us to join our talent community.