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Pharmacovigilance Summer Internships

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Showing 25–36 of 50 categories
Clinical Trial Safety Data Analysis Research
Conduct comprehensive safety analyses of clinical trial adverse events to support regulatory submissions and post-approval monitoring strategies.
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 →
Serious Adverse Event Triage Research
Develop classification and prioritization algorithms for serious adverse events to optimize regulatory resource allocation and investigation timelines.
5 focused areas Click to view more details →
Drug Withdrawal and Discontinuation Research
Investigate adverse events associated with medication discontinuation and withdrawal syndromes across different therapeutic drug classes.
5 focused areas Click to view more details →
Long-Term Safety Outcome Research
Study delayed and cumulative adverse effects from chronic drug exposure through longitudinal pharmacovigilance follow-up investigations.
5 focused areas Click to view more details →
Drug Labeling and Safety Communication Research
Research effectiveness of safety warnings, black box labels, and direct healthcare provider communications in reducing preventable adverse events.
5 focused areas Click to view more details →
Adverse Event Narrative Quality Research
Assess and improve the quality, completeness, and standardization of adverse event case narratives for regulatory assessment and signal detection.
5 focused areas Click to view more details →
Confounding Factor Analysis in Pharmacovigilance Research
Develop statistical methodologies to identify and control for confounding variables in observational pharmacovigilance safety analyses.
5 focused areas Click to view more details →
Cumulative Risk Assessment Research
Research methods for evaluating cumulative and combined risk of multiple medications used concurrently in individual patients.
5 focused areas Click to view more details →
Natural Product and Herbal Drug Safety Research
Study adverse events and safety concerns specific to botanical products, dietary supplements, and traditional medicines.
5 focused areas Click to view more details →
Biosimilar Safety Surveillance Research
Develop specialized pharmacovigilance approaches for monitoring safety outcomes unique to biosimilar pharmaceutical products.
5 focused areas Click to view more details →
Drug Contamination and Quality Defect Research
Investigate adverse events resulting from pharmaceutical manufacturing defects, contamination, and quality control failures.
5 focused areas Click to view more details →
Off-Label Use Safety Monitoring Research
Research safety profiles and adverse event patterns associated with off-label medication use in clinical practice.
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.