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Regional Medical Advisor

Abbott · Lucknow, India

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Medical AffairsFull-timeCompany career page

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Role summary

Abbott seeks an experienced Medical Affairs professional to oversee clinical trials and research activities in Lucknow. The role involves directing clinical protocols, managing investigator relationships, and ensuring regulatory compliance for phases III and IV trials.

What they're looking for

  • Associate's degree or equivalent educational qualification
  • Minimum 1 year of medical affairs or clinical research experience
  • Strong project management and protocol oversight skills
  • Ability to work with regulatory agencies and clinical investigators
  • Knowledge of adverse event reporting and safety monitoring procedures

What you'll be doing

  • Direct and oversee clinical trials phases III and IV for company products
  • Recruit clinical investigators and negotiate study design parameters
  • Implement clinical protocols and facilitate completion of final reports
  • Monitor protocol adherence and coordinate study completion activities
  • Manage adverse event reporting and coordinate regulatory submissions

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