Open to opportunities

Muzammil Khan

@muzammilkhan6

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Clinical drug development and pharmacovigilance intern building safety and medical documentation skills.

India

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What I'm looking for

I’m looking for a healthcare role in clinical drug development or pharmacovigilance where I can deepen ICH-GCP/GVP-aligned safety case work, adverse event workflows, and scientific documentation through hands-on exposure and structured training.

I’m a Clinical Drug Development Intern with exposure through the Global Healthcare Academy, working through Medical Affairs and Pharmacovigilance orientation on tools like Oracle Argus Safety, ARISg, and Veeva Vault Safety. I’ve supported mock safety case assessment by reviewing reportability, case validity, seriousness, expectedness, causality factors, and MedDRA terminology concepts.

I’m also building a foundation in ICH-GCP and GVP-aligned concepts like PSUR/PBRER, DSUR, Risk Management Plans, and benefit–risk assessment, while reviewing medical literature to support safety narratives and scientific documentation. Alongside this, I’m studying Executive Programs in Clinical Drug Development and Medical Affairs, and I’m looking for clinical research, pharmacovigilance, medical writing, and regulatory documentation-focused roles.

Experience

Work history, roles, and key accomplishments

Medical Affairs and Pharmacovigilance Intern

Academically Global Healthcare Academy

Jun 2025 - May 2026 (11 months)

Gained orientation on Oracle Argus Safety, ARISg, and Veeva Vault Safety, with exposure to safety database navigation and case workflow processes. Assisted in mock safety case assessment and developed understanding of adverse event reporting and pharmacovigilance regulations.

Oracle Argus Safety MedDRA ICH GCP GVP省令