
Independent Consultant
Seema Rajsingh
Senior Pharmacovigilance and Clinical Development Physician
Certifications
- Executive MBA, SP Jain School of Global Management
- Member, Lifesciences Australia (MMPP, MedTech and Pharmaceutical Professional)
- Member, Institute of Clinical Research (MICR), UK
- MD (Pharmacology), University of Delhi, India
- MBBS, Lady Hardinge Medical College, University of Delhi
Dr Seema Rajsingh is a medically qualified clinical development physician with over 25 years of experience across pharma, biotech, CRO and consulting settings. She has extensive expertise in medical monitoring and safety oversight across global Phase I–III clinical trials, including early phase, adaptive and complex trial designs, dose escalation and expansion studies, investigational medicinal products, advanced therapies and medical device-related clinical development.
Dr Rajsingh has held senior medical and safety roles involving investigator support, clinical development strategy, regulatory strategy, study governance, risk-based medical review and ICH-GCP compliant trial conduct. She has also supported safety review committees, dose escalation governance, DSMB/DMC interactions and safety decision-making in clinical trials.
In addition to medical monitoring, Dr Rajsingh has experience in pharmacovigilance, drug safety, PV and GCP audit support, SOP and process review, protocol development, clinical and scientific writing, safety narratives, clinical study reports and regulatory-facing clinical documents.
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