Clinical Scientific Expert I

1 - 4 years

3 - 7 Lacs

Posted:5 days ago| Platform: Foundit logo

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Work Mode

On-site

Job Type

Full Time

Job Description

  • Ensure high-quality clinical trial data review/insights and analysis as directed by the Integrated Clinical Trial Team (iCTT).
  • Perform thorough clinical data review and identify insights through patient-level review and trends analysis, supporting Interim Analysis, Database, and Post Lock activities.
  • Contribute to the development of the Data Review/Quality Plan (DRP/DQP) and data review strategy.
  • Support the development of study-level documents and contribute to pharmacovigilance activities if required.
  • Produce training materials and provide training to iCTT.

Role Requirement:

  • Education:

    Advanced degree in life sciences/healthcare (or clinically relevant degree) required.
  • Experience:

    >1 year experience in pharmaceutical industry/clinical research organization preferred.
  • Skills:

    Strong analytical skills, knowledge of clinical trial design, statistical analysis, and regulatory processes. Fluent in English (oral and written).

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