Nasser Khan
Product Safety Lead @ Daiichi Sankyo US | Clinical Safety and Pharmacovigilance (CSPV)
- Role
- Product Safety Lead at Daiichi Sankyo US
- Location
- North Chicago, IL, US
- LinkedIn followers
- 500 followers
About Nasser Khan
My name is Nasser Khan and I am a seasoned and accomplished professional with 25+ years of pharmacovigilance experience in driving clinical strategies, pioneering advancements in infectious/inflammatory disease treatment, and developing groundbreaking therapeutic products.Throughout my career, I have developed solid skills and achieved out-of-the-box results.• Repeated success in aligning medical services with defined organizational goals and implementing evidence-based practices.• Prudent in steering transformative initiatives, championing clinical excellence, and streamlining operational efficiency.• Skilled in analyzing data, identifying trends, and providing actionable insights for decision-making and process improvement.• Astute in managing and monitoring patient safety across all phases of clinical trials and delivering quality safety regulatory documents.• Visionary leader with proven expertise in leading, mentoring, and coordinating staff, through effective management of organizational diversity.My areas of expertise include:· Patient Safety & Clinical Trials· Clinical Strategy Development· Therapeutic Area & Competitor Analysis· Pharmaceutical Research Management· Strategic Planning & Execution· Clinical Education & Outreach· Relationship Building & Growth· Quality Assurance & Control· Policies & Procedures Compliance· Cross-Functional Collaboration· Interpersonal Communication· Operational ExcellenceFeel free to reach out to me via email @ n•••••@gmail.com.
Experience
Product Safety Lead
May 2024 — Present · North Chicago, IL, US
Product Safety Lead for early development compounds and marketed drugs.
Education
Nishtar Medical College
Bachelor of Medicine, Bachelor of Surgery - MBBS, Medicine
Skills
- Medical Writing
- Clinical Monitoring
- Oncology
- Diabetes
- Clinical Study Design
- Ich-Gcp
- Meddra
- Pharmaceutical Industry
- Drug Safety
- Medical Affairs
- Clinical Data Management
- Medicine
- Pharmaceutical Research
- Clinical Trials
- Pharmacovigilance
- Regulatory Submissions
- Clinical Operations
- Drug Development
- Gcp
- Metabolism
- Clinical Development
- Endocrinology
- Immunology
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