FIND_THE_RIGHTJOB.
India
IQVIA is looking for candidates who have expertise in regulatory writing to join our Real World Evidence team. The Ideal candidate will have 5-12 years of experience working as Regulatory Medical Writer, adept in developing and authoring clinical study protocols, informed consent documents, clinical study reports.
Expectations:
Education & Experience:
Master’s degree or PhD in the field of healthcare (e.g. Bio-medical sciences/ life sciences/ Pharmacy/ Bio-Tech, MBA in Pharmaceutical Management etc.)
Experience – 8 to 12 Years
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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