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Pharmacovigilance Internships

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Pharmacovigilance Internships with Accommodation

Explore internship opportunities with access to NTHRYS accommodation options at active branch locations in India.

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.
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