Job Number
Job Category
Clinical Research Associate
Position Type

Job Overview

CRA, Clinical Research Associate Job, Jobs. Phase 1 clinical trials. Barcelona. Madrid. Oncology





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 have helped the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today and 100 % of all Oncology drugs approved in 2016.


Explore this CRA job with Covance Early Clinical Development and check for yourself why we are known to promote 2.5x more employees annually than the average company in the sector.





Can you bring your drive to our cutting-edge clinical projects?


We need experienced CRAs who are ready to apply their pre-study, initiation, monitoring and closeout visits expertise, and their deep ICH-GCP and SAE management expertise to bring safe, effective and essential medicines to market sooner.


Location: Madrid or Barcelona (home based)


This job opportunity is to work within our Early Clinical Development team, and you will be engaged with Ph 1 trials in oncology.



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



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




You are a CRA with 3-4 years of validated independent monitoring experience in international phase I clinical trials (initiation, routine & close out visits, SAE reporting, etc.) Having monitored oncology trials is needed.


You are working at an international CRO or Pharma, and are fluent in English




Want to enquire about our salary range, flexible timetable, holidays, health and other benefits? Please contact us to discuss.



Join us and see why Covance has been named among the World´s Most Innovative Companies in Forbes´ 2017 Ranking, and more than 90% of the top 20 global pharmaceutical companies are repeat customers… We can offer you not only a job, but a stable, long-term international career.  


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, Carlos Villanueva, to discuss in confidence:





More about us: 







Education / Qualifications

  • University/college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology).
  • Thorough knowledge of ICH guidelines, GCP and the clinical trial process
  • Knowledge of the drug development process.
  • Proficient computer skills with good working knowledge of a range of computer packages including Electronic CRF processes.
  • Excellent verbal and written communication skills
  • Valid Drivers License


- 3-4 years of experience in a related field, including 2-3 years of independent on-site monitoring in CRO or Pharma

- Experience with Phase I and PoC Studie


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