Clinical Trial Specialist

2 days ago


Bengaluru, Karnataka, India beBeeScientific Full time ₹ 15,00,000 - ₹ 25,00,000

Job Overview

  • Develop high-quality clinical trial documents, including protocols and study reports.
  • Translate complex scientific data into clear, regulatory compliant documents.

Key Responsibilities:

  1. Create key clinical trial documents such as protocols, investigator's brochures, informed consent forms, case report forms, and clinical study reports.
  2. Communicate complex scientific data in a clear, concise manner to support drug development and approval processes.
  3. Craft abstracts and manuscripts demonstrating strong scientific writing skills.

Additional Duties:

  1. Prepare protocols, clinical study reports, patient information sheets, and case report forms.
  2. Understand study objectives and design protocols accordingly.
  3. Develop and review standard operating procedures.
  4. Collaborate with stakeholders to ensure complete documentation within timelines.

Requirements:

  • Proficiency in developing high-quality clinical trial documents.
  • Ability to translate complex scientific data into clear documents.
  • Strong scientific writing skills.
  • Ability to deliver accurate and well-structured documents.


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