CRA II or Senior CRA - Sponsor Dedicated -FSP
- Employer
- Labcorp
- Location
- Rome, Italy
- Salary
- Competitive
- Start date
- 11 Sep 2019
- Closing date
- 8 Oct 2019
View more
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Apply now and receive a generous welcome bonus
The Job:
- Office or Field based, home office: strong preference Rome / Milan; other well connected cities (i.e. Bologna, Firenze, Napoli, Bari, etc) can be considered for the right person.
- 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; computer literacy)
- Good organizational and time management skills, able to work highly independently
- Flexibility, expected travelling is 2-3 days per week
- Fluent in Italian and English (verbal and written)
What makes this opportunity special?
- Competitive salary, car allowance and benefits package, including lunch vouchers, etc.
- Career progression will be exceptional because there are lots of studies coming through in 2019, so you will strength your oncology clinical monitoring skills fast
- You will be 100% client focused with a prestigious Pharmaceutical company.
- Unlike some CRA roles you will not be pushed to satisfy unrealistic \u2018monthly visit\u2019 targets
- The job is permanent and full time
- You will be joining a large team with a well organised structure and robust processes in place
Other Information:
This role is afull time & permanent position to beemployed by Covance.
Education/Qualifications:
- University or college degree, or certification in related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
- Valid Driver\u2019s License B
- Thorough knowledge of CGP-ICH and basic understanding of the regulatory requirement
- At least 2 years of independent monitoring experience, including oncology Phases I, II and III trials
- Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- Previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) in Italy.
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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