Sara Iqbal is an experienced regulatory professional currently serving as a Regulatory Manager at Pharmaron since October 2020, where responsibilities include the implementation and maintenance of electronic Trial Master Files (eTMF), supervising Regulatory Associates, and overseeing project management within drug development processes. Previously, Sara held roles as a Regulatory Specialist and Clinical Research Coordinator, demonstrating a strong background in regulatory submissions, patient management in clinical trials, and compliance with FDA regulations and Good Clinical Practice. Earlier work experience includes roles in medical assistance and health insurance consulting, supported by an MD from Ross University School of Medicine and a Bachelor's degree in Biology from Springfield College.
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