Pharmacovigilance - Internship (WFH)

About the internship:Selected intern's day-to-day responsibilities include:

1. Learn the fundamentals and importance of pharmacovigilance.

2. Understand adverse drug reactions (ADRs) and adverse events.

3. Learn the process of identifying, documenting, and reporting safety information.

4. Understand Individual Case Safety Reports (ICSRs).

5. Learn the basics of case intake, data entry, and case processing.

6. Understand the concepts of seriousness, expectedness, and causality assessment.

7. Learn about follow-up information and case reconciliation.

8. Understand the importance of drug safety databases and safety documentation.

9. Gain exposure to pharmacovigilance regulations and reporting requirements.

10. Work on sample safety cases and practical case studies.

11. Identify and analyze safety-related information from provided scenarios.

12. Apply the acquired knowledge to a pharmacovigilance capstone project during the third month.Who can apply:Only those candidates can apply who:are available for the work from home job/internshipcan start the work from home job/internship between 16th Sep'26 and 21st Oct'26are available for duration of 3 monthshave relevant skills and interestsStipend:INR₹ 8,000 - 20,000 /monthDeadline:[hidden]:59:59Other perks:Certificate, Letter of recommendation, Flexible work hours, 5 days a weekSkills required:Effective CommunicationOther Requirements:Candidates must be from Pharmacy background only.About Company:Simpli Intern is a global online bootcamp and digital skills training provider that helps working professionals and students learn in-demand technical fields. It offers courses and certifications in fields like data science, AI, cyber security, and project management through partnerships with top universities and companiesAdditional information:

Stipend Structure:

Fixed pay: ₹ 5,000 - 15,000 /month

Incentive pay: ₹ 3,000 - 5,000 /month

Responsibilities

Selected intern's day-to-day responsibilities include:

1. Learn the fundamentals and importance of pharmacovigilance.

2. Understand adverse drug reactions (ADRs) and adverse events.

3. Learn the process of identifying, documenting, and reporting safety information.

4. Understand Individual Case Safety Reports (ICSRs).

5. Learn the basics of case intake, data entry, and case processing.

6. Understand the concepts of seriousness, expectedness, and causality assessment.

7. Learn about follow-up information and case reconciliation.

8. Understand the importance of drug safety databases and safety documentation.

9. Gain exposure to pharmacovigilance regulations and reporting requirements.

10. Work on sample safety cases and practical case studies.

11. Identify and analyze safety-related information from provided scenarios.

12. Apply the acquired knowledge to a pharmacovigilance capstone project during the third month.