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Mgr Clinical Research

Zoek Pin Bengaluru, Karnataka

Permanent (Full time)

Posted 14 days ago

Job Description

  • To ensure that the clinical study is conducted according to the approved protocol and applicable regulatory requirements.
  • To protect rights, safety and welfare of subjects.
  • Management of Investigational Products.
  • To ensure that sufficient number of qualified medical, paramedical, and clerical staff is available to conduct the study.
  • To ensure that all staff assisting in study is adequately trained on the protocol, investigational product and their duties.
  • To be aware of regulatory requirements and acceptable standards for conduct of clinical trial and protection of human subjects.
  • To ensure that the data is complete, accurate, legible and internally consistent and maintain timelines.
  • To take all study related medical decisions.
  • To ensure that adequate medical care is provided to the subject for any adverse event, including clinically significant laboratory values.
  • In case of health related problems, the investigator should inform the subject's primary physician about the subject's participation in the trial, if the subject has a primary physician and if the subject agrees to the primary physician being informed.
  • To Review AE / SAE reporting forms after it is filled by the physician / designee.
  • To Provide timely inputs on the protocol


  • 7+ years of experience either with MBBS/MD

Research & Development

Sub Function
Clinical Research

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