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CLINICAL RESEARCH ASSOCIATES, SPAIN

Employer
Labcorp
Location
Madrid, Spain;Barcelona, Spain
Salary
Competitive
Start date
8 Oct 2019
Closing date
24 Oct 2019

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Job Details

Wide varietyof CRA II & SCRA jobs in Spain: client dedicated or working in-house on Covance studies



Generous Welcome Bonus if you join us now!



Top 5 pharmaceutical clients



Therapeutic experience required: Oncology & Infectious diseases/ HIV





WHERE WILL YOUR CURIOSITY TAKE YOU?



Covance Spain offers unique job opportunities to gain exposure across the broadestoncology/ Infectious diseases clinical trial portfolios. Whether your ambition is to work sponsor dedicated or with different clients, we have the right job for you.



Covance Spain are living an unprecedented growth so we are in the position of offering a wide variety of Clinical Research Associate II (CRA II) and Senior Clinical Research (SCRA) job opportunities:


  • Sponsor dedicated: experience the stability of working with just one sponsor company and being part of two families who are both interested in your development and welfare.


  • Covance Clinical Solutions: today's 50 top-selling FDA approved drugs were supported by Covance. By working in-house on Covance studies, you will be immersed in the tools and processes that have allowed us tosuccessfully conduct over 720 oncology trials since 2012 in over 75 countries





WHAT MAKE THESE JOBS SPECIAL?



No matter which team you chose you will experience:


  • Generous Welcome Bonus if you start the recruitment process now!


  • Career progressionwill be exceptional: unlike other CROs, there are not fixed boundaries between our teams: we offer flexibility with great opportunity togrowinto a variety of areas such as Project Management, Clinical Team Leadership, Line Management and cross border roles.


  • Unlike some CRA roles you will not be pushed to satisfy unrealistic \u2018monthly visit' targets


  • With us, you will become anexpert in oncology/infectious diseasestrials, learning how to overcome the complexities and challenges of oncology drug development and how to prevent the pitfalls that derail many onco trials.


  • Competitive salary and benefits package, including lunch vouchers and flexi time


  • You will be joining a large team with a well organised structure and robust processes in place





Our employees make a difference in the lives of millions of people\u2026 and you will too.



Join us and see why LabCorp/ Covance have been named for the second consecutive year to FORTUNE\u00B4s 2019 List of `World\u00B4s Most Admired Companies\u00B4 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.







THE CRA JOB:



In terms of location:



We need you to be based inMadrid/Barcelona, and we can offer you to participate in a wide variety of:


  • Oncology trials: all indications and phases, and we have special need for CRA experts in monitoringph Iandlung cancerstudies


  • Infectious diseases/ HIV





In terms os skills:
  • Previous monitoring experience in multicenter oncology/ Infectious diseases clinical trials is needed -minimum 2 years
  • Proven skills in site management including site performance and patient recruitment
  • Excellent soft skills (include oral and written communication skills in Spanish and English; computer literacy)
  • Good organizational and time management skills, able to work highly independently



OTHER INFORMATION



These jobs are full time & permanent positions to be employed through Covance. For more information please contact Carlos Villanueva on +34 648 853 615 or mailcarlos.villanueva@covance.com
Education/Qualifications:
University degree, life science.



Extensive knowledge of:
  • Drug development process and client needs.
  • ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
Experience:
Extensive clinical monitoring experience in Spain is needed, minimum 2 years monitoring studies in Oncology/ Infectious diseases/HIV with proven track record of pre-study, initiation, routine monitoring and closeout visits.



Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines



Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs



Ability to resolve project-related problems and prioritize workload for self and team



Advanced site monitoring &study site management skills

Ability to work with minimal supervision

Good planning and organization skills

Good computer skills with good working knowledge of a range of computer packages


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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