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Pharm.D intern with hands-on clinical exposure and strong interest in clinical research, pharmacovigilance, and drug safety. Published researcher with additional training in molecular docking and multiple certifications in clinical research methodologies. Seeking opportunities to contribute to evidence-based healthcare and patient safety in the pharmaceutical and clinical research industry.

I am a detail-oriented B.Pharmacy graduate with a solid foundation in pharmacovigilance and clinical data management. My skills include signal detection, adverse event analysis, and ensuring regulatory compliance. I am adept in case processing, medical coding, and data management tools. My academic training has equipped me with the knowledge of drug safety reporting and patient counseling, aiming to enhance patient safety in my future roles.

A driven PharmD graduate with a strong background in pharmacovigilance, adverse drug reaction (ADR) reporting, and clinical research and can bring practical experience in patient counseling, medication auditing, and clinical pharmacy. Experienced in completing clinical reviews, counseling patients and supporting physicians with information about appropriate dosages and protocols. Well-versed in medication contraindications, interactions and side effects. Seasoned Clinical Pharmacist adept at providing evidence-based recommendations to physicians. Proficient in reporting, documentation and compliance guidelines. Focused on maintaining current knowledge of therapeutic options. Logical PV Expert with background identifying, assessing and preventing adverse effects or medications, vaccines and related pharmaceutical items. Dedicated expert with focus on maintaining drug safety by preparing and reviewing data and reports. Meticulous when authoring professional documents and reviewing scientific literature.

Pharm D graduate with hands-on experience in Clinical Data Collection/Management, Pharmacovigilance, Medical Writing and Clinical Research. Core competencies include EDC system, CRF review, ADR Reporting (Vigiflow) and ICH-GCP ( E6-R2) guidelines, clinical workflow. Seeking an entry-level role in Clinical research, Pharmacovigilance or Clinical Data Management.

MOHAMMED SULAIMAN KHAN

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Doctor of Pharmacy (Pharm.D) -

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Pharm.D Intern

Doctor of Pharmacy (Pharm.D) -

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