CLINICAL RESEARCH ASSOCIATES, ITALY
- Employer
- Labcorp
- Location
- Rome (IT)
- Salary
- Competitive salary, car allowance and benefits package, including lunch vouchers
- Start date
- 8 Oct 2019
- Closing date
- 7 Nov 2019
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- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Wide variety of CRA II - SCRA jobs in Italy: 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
WHERE WILL YOUR CURIOSITY TAKE YOU?
Covance Italy offers unique job opportunities to gain exposure across the broadest oncology clinical trial portfolio. Whether your ambition is to work sponsor dedicated or with different clients, we have the right job for you.
Covance Italy is 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 to successfully 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 progression will be exceptional because unlike other CROs, there are not fixed boundaries between teams: we offer flexibility with great opportunity to grow into 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 ‘monthly visit’ targets
- With us, you will become an expert in oncology, 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, car allowance and benefits package, including lunch vouchers
- 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… and you will too.
Join us and see why LabCorp-Covance have been named for the second consecutive year to FORTUNE´s 2019 List of `World´s Most Admired Companies´ 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:
Location:
- Rome and Milan are our ideal cities.
- For some jobs we can also consider other well connected cities (i.e. Bologna, Firenze, Napoli, Bari), but for these we can only consider well experienced CRAs used to work home-based.
Skills:
- Previous monitoring experience in oncology 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 Italian 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 .
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 Italy is needed, minimum 2 years monitoring studies in Oncology, 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
Excellent understanding of Serious Adverse Event (SAE) reporting
Ability to resolve project-related problems and prioritize workload for self and team
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.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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