Anushka Hemant Bhadra English, Writing, Speaking
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Am a Regulatory Affairs professional with a strong academic foundation in Bachelor’s in Pharmacy, complemented by hands-on experience supporting regulatory and clinical research activities. I have worked across regulatory documentation, compliance support, and cross-functional coordination, ensuring adherence to FDA, ICH-GCP, and institutional guidelines. My experience includes preparing and reviewing regulatory submissions, maintaining essential documents, supporting audits and inspections, and collaborating with clinical and quality teams to ensure regulatory readiness.

With a patient-focused mindset and a strong understanding of drug development and regulatory pathways, I bring a detail-oriented and organized approach to regulatory operations. I am highly motivated to contribute to roles that support product compliance, clinical trial oversight, and regulatory strategy while continuing to grow within the pharmaceutical and biotech industry.In addition to my academic and professional background, I have successfully appeared for competitive examinations such as NEET, IELTS, and CAT, which have strengthened my foundation in scientific concepts, analytical reasoning, and English language proficiency. This background enables me to effectively interpret scientific data, prepare clear regulatory documentation, and communicate confidently with cross-functional and global stakeholders.

Subjects

  • English Beginner-Expert

  • English Grammar Beginner-Expert

  • Geography (English Medium) Beginner-Expert

  • Science (Biology, Chemistry, Physics) Beginner-Expert

  • English & Literature Beginner-Expert

Experience

No experience mentioned.

Education

  • MS in Regulatory Affairs (Jan, 2023–Dec, 2024) from Northeastern University, Boston, MA, USA
  • Pharmacy (Aug, 2018–May, 2022) from Bachelor's in pharmacy

Fee details

    ₹1,000–1,500/hour (US$10.53–15.79/hour)

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