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- You must have an advanced science degree (PharmD, PhD or MD, etc) and two (2) years or more corporate/business experience required or equivalent combination of education and experience required.
- Two (2) or more years relevant pharmaceutical/medical writing experience required in a medical communications agency.
- Excellent demonstrable understanding of ICMJE and GPP guidelines and regulations required.
- Ability to read, analyze, and interpret common scientific and technical journals.
- Ability to respond to common inquiries or complaints from customers.
- Ability to write presentations and articles for peer reviewed publications that conform to prescribed style and format.
- Must demonstrate a command of the English language (read, write and speak).
- Ability to work with mathematical concepts such as probability and statistical inference.
- To perform this job successfully, an individual should have knowledge of Internet software, Spreadsheet software, Word Processing software, Graphics software (eg, PowerPoint or Prism), Biliographic software eg, EndNote) and any other applicable software as may be needed by the job from time to time as it changes.
- Must demonstrate strong experience in relationship-building and experience in collaborating with large and strategic accounts.
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Who we are
Salary
Location
France, Paris
Department
Clinical Monitoring
Location
Paris
Lyon
Remote Working
Hybrid: Office/Remote
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
InHouse CRA (Fast Track to CRA)France, Officebased in Paris or Lyon.At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to f
Reference
JR115273
Expiry date
01/01/0001
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UK, Reading
Remote Working
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Location
Argentina
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Location
Belgium, United Kingdom, Denmark, France, Spain, Germany, Netherlands, Switzerland
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Location
Belgium
Denmark
France
Germany
Netherlands
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Reference
2023-103952
Expiry date
01/01/0001
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