Medical Writer - BA/BE Studies

1 - 6 years

7 - 14 Lacs

Posted:10 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Role & responsibilities

  • Preparation and Compilation of Study Proposal Synopsis.
  • Literature survey and preparation and review of Clinical Study Protocols as per sponsor and / or applicable regulatory authorities.
  • Preparation and Compilation of Clinical Study reports.
  • Regular interaction with the Investigators of various departments for protocol inputs.
  • Preparation of informed consent documents and protocol associated appendices.
  • Handling and providing responses to sponsors and regulatory queries.
  • Responsible for Review of regulatory guidelines with the current requirements for clinical research services related activities.
  • Review procedures for pharmacy operations.

Preferred candidate profile

M.Pharm (Pharmacology) with 1-6 Yrs with relevant experience

Interested candidates can share their CVs on:

meghamaheshwari@torrentpharma.com / vilshashah@torrentpharma.com

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Torrent Pharmaceuticals logo
Torrent Pharmaceuticals

Pharmaceutical Manufacturing

Ahmedabad Gujarat

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