ASCEND BY NTHRYS
Research Abroad Products

Pharmacovigilance Winter Internships

Click a category to proceed further.

Showing 13–24 of 50 categories
Rare Adverse Event Identification Research
Research statistical approaches and algorithms specifically designed to identify rare and previously unreported adverse drug reactions.
5 focused areas Click to view more details →
Drug Safety Database Integration Research
Study methods for integrating and harmonizing data from disparate pharmacovigilance sources including FDA, EMA, and national regulatory databases.
5 focused areas Click to view more details →
Causality Assessment Algorithm Development Research
Design and validate computational algorithms to automatically determine causal relationships between drugs and adverse events using standardized assessment scales.
5 focused areas Click to view more details →
Medication Error Reporting System Research
Analyze medication error data collection systems and develop improved reporting mechanisms to prevent drug-related incidents in clinical settings.
5 focused areas Click to view more details →
Genotoxicity and Mutagenicity Assessment Research
Research laboratory methods and in vitro testing protocols to assess potential genotoxic and mutagenic risks of pharmaceutical compounds.
5 focused areas Click to view more details →
Hepatotoxicity Risk Prediction Research
Develop predictive models and biomarker identification strategies to assess drug-induced liver injury risks during preclinical and clinical phases.
5 focused areas Click to view more details →
Nephrotoxicity Monitoring and Research
Study renal safety biomarkers and surveillance methods to detect and prevent drug-induced kidney damage in patient populations.
5 focused areas Click to view more details →
Cardiotoxicity Early Detection Research
Investigate emerging cardiac biomarkers and monitoring technologies for early identification of drug-induced cardiovascular adverse events.
5 focused areas Click to view more details →
Pharmacogenomics Safety Interaction Research
Research genetic biomarkers and polymorphisms that influence individual susceptibility to specific adverse drug reactions and drug interactions.
Academic (A)Tech (T)Research (R)
1 Month
A · ₹7,670
T · ₹36,798
R · ₹53,525
3 Months
A · ₹48,387
T · ₹59,140
R · ₹86,022
6 Months
A · ₹1,07,528
T · ₹1,31,423
R · ₹1,91,160
14 more durations from 5 days to 1 year
5 focused areas Click to view more details →
Drug-Disease Interaction Safety Research
Analyze how underlying patient comorbidities and disease states influence adverse drug reaction risks and pharmacovigilance surveillance strategies.
5 focused areas Click to view more details →
Population Subgroup Safety Analysis Research
Examine safety profiles across diverse demographic groups including geriatric, pediatric, and ethnically diverse populations using stratified pharmacovigilance data.
5 focused areas Click to view more details →
Pregnancy and Lactation Drug Safety Research
Study adverse event outcomes in pregnant and nursing populations and establish safety registries for medications used during pregnancy.
5 focused areas Click to view more details →
Looking for internship topics in Pharmacovigilance? Explore all Pharmacovigilance internship topics and focused areas available across our internship categories.