SUMMARY OF POSITION

Do you have a strong interest in pharmaceuticals and drug safety? We are seeking a highly motivated student seeking hands-on experience in drug safety processes, case management, and regulatory reporting. Our Pharmacovigilance intern will have the opportunity to contribute to patient safety initiatives while learning foundational drug safety skills across several therapeutic areas. If you are a self-starter with a strong attention to detail and a desire to learn and grow, we encourage you to apply for this exciting opportunity.

ORGANIZATION STRUCTURE

This position will report to the Medical Director, USPV - Alvogen and will work in close partnership with members of the Drug Safety, Research and Development, Clinical Operations, Quality Operations, and training teams.

RESPONSIBILITIES

Primary responsibilities of this role include the following:

• Participate in drug information research and presentation sessions
• Assist with implementing safety programs across functional teams
• Assist with the review of safety data reports and perform data analysis
• Research and understand disease, symptoms, and standard management
• Participate in literature analysis and discussions related to pharmacovigilance strategies and initiatives

Expectations:

• Interest and experience in Biologics and Drugs
• Ability to work on site Tuesday - Thursday.

QUALIFICATIONS

Minimum Qualifications:

• Currently pursuing a Pharm.D or a Bachelor's in Science
• Excellent analytical/statistical skills
• Ethics, professionalism, and an interest in the biopharmaceutical industry
• High school diploma or GED Comfortable with computers and the use of MS Office Suite programs

GMP DECISION-MAKING AUTHORITY

N/A

The anticipated base hourly range for this position is $20. We anticipate this position will be posted on April 14, 2026, and remain open for at least 10 days. To apply, select the apply button and submit your application.

An Equal Opportunity Employer, including disability/vets.