Job Description

Key Responsibilities

Clinical Protocol Review

  • Assist in the review and understanding of clinical study protocols, informed consent forms, and related study documents.
  • Support identification of protocol deviations, inconsistencies, and missing information.
  • Coordinate with senior team members for protocol clarifications and updates.
  • Maintain accurate documentation as per SOPs and regulatory guidelines.

Literature Search & Medical Writing Support

  • Conduct systematic literature searches using scientific databases (PubMed, Google Scholar, etc.).
  • Summarize published clinical data, safety information, and therapeutic background.
  • Assist in preparing literature review reports, study summaries, and reference documents.
  • Ensure proper citation and version control of documents.

Clinical Study Monitoring Support

  • Support clinical trial monitoring act...

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