5 - 10 years

7 - 15 Lacs

Posted:5 days ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Role & responsibilities

  • Collaborate with clinical and research teams to design clinical trials, including statistical analysis plans and sample size calculations.
  • Perform statistical analyses of clinical trial data using appropriate statistical methods and software.
  • Prepare statistical reports, summaries, and contribute to the writing of regulatory submissions, manuscripts, and presentations.
  • Ensure the accuracy and integrity of data through comprehensive reviews and validation of datasets.
  • Provide guidance to CDM in preparation of CRF designing and identification of critical

data points and data validation.

  • Work closely with Global Medical Affairs biostatisticians to identify statistical analysis needs and assist in developing assigned deliverables.

Preferred candidate profile

Demonstrate strong written and verbal communication skills.

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