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Senior Medical Writer

MS CLINICAL RESEARCH

Bengaluru / Bangalore

Not Disclosed

3 - 5 Years

Full Time - Permanent

Views:260

Applicants:8

Posted on 21 Jul, 2024

In Office

Job Description | Responsibilities

  • You'll write and review documents for clinical trials, making sure they're accurate, meet regulations, and explain things clearly.
  • You'll collaborate with other experts to ensure all the information is there and makes sense.
  • You'll interpret complex data from studies and scientific literature, then explain it in a way that's easy to understand.

Overview

  • Industry - CRO, Clinical Research Organization
  • Functional Area - Research / R&D - Pharma / Medical / Health / Biological Sciences
  • Job Role - Other Top Management R&D / Research - Pharma / Medical / Health / Biological Sciences
  • Employment type - Full Time - Permanent
  • Work Mode - In Office

Qualifications

  • Any Graduate - Any Specialization
  • Any Post Graduate - Any Specialization
  • Any Doctorate - Any Specialization

Job Related Keywords

Medical Coding Concept Development Computer literacy Physiology Policiesw & procedures Reporting