Intern Pharmacovigilance

OpenSafety; Colombia; Remote; COP 13,392,000 - 26,784,000; Full time

Benefits offered by this job

Remote work

Job summary

OpenSafety in Colombia is seeking a motivated Pharmacovigilance Intern to support safety data review, case processing, and signal detection activities. This remote full-time role is ideal for fresh graduates looking to gain hands-on experience in drug safety.

You will assist in literature screening for ADRs, data entry of ICSRs, and preparation of safety reports while ensuring regulatory compliance and patient safety.

Qualifications

• Bachelor's or Master's in Pharmacy or Life Sciences.
• Basic understanding of Pharmacovigilance concepts.
• Good knowledge of medical terminology.
• Strong attention to detail.
• Good communication and analytical skills.
• Familiarity with MS Excel and data entry.

Responsibilities

• Literature screening for adverse drug reactions (ADRs).
• ICSR data entry and processing assistance.
• Support signal detection and evaluation activities.
• Maintain accurate documentation of safety data.
• Assist in preparing safety reports and summaries.
• Ensure compliance with pharmacovigilance guidelines.

Skills

Attention to detail

Communication skills

Analytical thinking

MS Excel

Education

Bachelor’s or Master’s degree in Pharmacy or Life Sciences

Tools

MS Excel

Job description

We are seeking a motivated Pharmacovigilance Intern to support safety data review, case processing, and signal detection activities. This role is ideal for freshers looking to gain hands‑on experience in drug safety.

Remote Full-time

Description

As a Pharmacovigilance Intern, you will assist in monitoring drug safety data, reviewing literature, and supporting case processing activities. You will work closely with the safety team to ensure compliance with regulatory requirements and contribute to maintaining patient safety.

Responsibilities

• Perform literature screening for adverse drug reactions (ADRs)
• Assist in Individual Case Safety Report (ICSR) data entry and processing
• Support signal detection and evaluation activities
• Maintain accurate documentation of safety data
• Assist in preparing safety reports and summaries
• Ensure compliance with pharmacovigilance guidelines

Requirements

• Bachelor’s or Master’s degree in Pharmacy or Life Sciences
• Basic understanding of Pharmacovigilance concepts
• Good knowledge of medical terminology
• Strong attention to detail
• Good communication and analytical skills
• Familiarity with MS Excel and data entry