Summer Pharmacovigilance Intern: Drug Safety Training

Southern Arkansas University

California (MO)

Hybrid

USD 20,664 - 27,552

Full time

14 days+
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Job summary

Southern Arkansas University is seeking a Pharmacovigilance Intern for a Summer 12-week program in California. This internship offers hands-on experience in drug safety and pharmacovigilance processes while participating in a structured training curriculum. Responsibilities include managing adverse events, assisting in safety data review, and completing a capstone project. Ideal candidates are currently enrolled in a life science program, have a strong interest in drug safety, and possess good communication skills. Options for hybrid or remote work are available.

Qualifications

  • Current enrollment in a bachelor’s, master’s, PharmD, MD, or related life science program.
  • Strong interest in drug safety, clinical research, or regulatory science.
  • Basic understanding of clinical research concepts and medical terminology.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple tasks and seek guidance appropriately.

Responsibilities

  • Support the Drug Safety/Pharmacovigilance (PV) team in adverse event management.
  • Assist with classification of adverse events and adverse drug reactions.
  • Participate in review of pharmacovigilance SOPs and GCP modules.
  • Complete a capstone project and present findings to the team.

Skills

Interest in drug safety
Basic understanding of clinical research
Excellent communication skills
Ability to work collaboratively

Education

Current enrollment in a life science program

Job description

Southern Arkansas University is seeking a Pharmacovigilance Intern for a Summer 12-week program in California. This internship offers hands-on experience in drug safety and pharmacovigilance processes while participating in a structured training curriculum. Responsibilities include managing adverse events, assisting in safety data review, and completing a capstone project. Ideal candidates are currently enrolled in a life science program, have a strong interest in drug safety, and possess good communication skills. Options for hybrid or remote work are available.
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