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Clinical Research Associate II

Employer
Labcorp
Location
Geneva, Switzerland
Salary
Competitive
Start date
26 Sep 2019
Closing date
26 Oct 2019

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Job Details

Covance is searching for aCRA IIto be home based in Switzerland

At Covance, we value your unique point of view and bold ideas to help bring innovative medicines to market and advance modern healthcare. Join our supportive team and see how our flexible work environment along with mentoring, training and career development can help you thrive personally and professionally.

Together, let's shape new possibilities for your career and improve the lives of patients around the world.

Covance is committed to diversity in the workplace and is an equal opportunity employer.



Are you an organized person who can work independently and take ownership of your career? Would you like to gain on-the-job skills while helping advance life-changing medicines?

If you are looking to enter a nurturing environment that provides a clear path to advancement, consider furthering your career as a Covance Clinical Research Associate (CRA).



In this role, you will:
  • Support large, prominent pharmaceutical company with their clinical trials
  • Have opportunity to gain experience in monitoring oncology and other indications studies
  • Ability to monitor in DACH
  • Oversee site monitoring with remote and in-person visits
  • Work in a flexible environment with a close-knit team
  • Use time management and people skills to ensure complianceWorking both field and home-based, our CRAs form strong connections with a team that works together to achieve shared success.
Education/Qualifications:
  • Bachelor or Master degree in life sciences
Experience:
What we're looking for

CRAs are the most successful at Covance with at least two years of clinical monitoring experience along with:
  • Familiarity with following Standard Operating Procedures, ICH guidelines and GCP
  • Experience conducting pre-study, site initiation, routine monitoring and close out visits
  • Ability to negotiate study budgets with investigators and assist the Covance legal department with statements of agreements
  • Deep understanding of Serious Adverse Event (SAE) reporting
  • Therapeutic experience including but not limited to cardiovascular, diabetes, oncology, infectious disease, neuroscience, metabolism and vaccines
  • A valid driver's license
  • Fluency in English, German and/or good knowledge in Italian and French


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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