Tamheer Training Opportunity | Pharmacovigilance (PV) Trainee

TalentLyft; Jeddah; On-site; SAR 36,000 - 58,000; Full time

Job summary

Jamjoom Pharma invites applications for a Tamheer training opportunity as a Pharmacovigilance (PV) Trainee in Jeddah, Saudi Arabia. You will work under the supervision of the QPPV to gain practical exposure to day-to-day PV activities.

Responsibilities include ICSR processing, literature screening, signal detection, and preparation of PV documentation. The program emphasizes learning, confidentiality, and cross-functional collaboration with Regulatory, Quality, and Medical Affairs.

Qualifications

• Bachelor's degree in pharmacy or PharmD is required.
• Fresh graduate with interest in Pharmacovigilance and Drug Safety.
• Good communication and organizational skills.
• Good command of English.
• Proficiency in Microsoft Office.
• Attention to detail and analytical thinking.
• Willingness to learn and maintain confidentiality.
• Tamheer eligibility must be met.

Responsibilities

• Support ICSR processing, including data entry and narrative preparation.
• Assist with case follow-up and collection of missing safety information.
• Assist with safety case processing and reporting within regulatory timelines.
• Maintain PV records and safety databases.
• Support literature screening and signal detection activities.
• Coordinate with Regulatory, Quality, and Medical Affairs on PV tasks.
• Participate in PV training and SOP/compliance activities.

Skills

Communication

Organizational

Analytical thinking

Confidentiality

English

Attention to detail

Learning ability

Medical knowledge

Education

BSc Pharmacy or PharmD

Tools

Microsoft Office

Job description

Location: Jeddah, Saudi Arabia

Jamjoom Pharma is offering a Tamheer training opportunity for a Pharmacovigilance (PV) Trainee to gain practical, hands-on exposure to day-to-day pharmacovigilance activities under the supervision and guidance of the Qualified Person for Pharmacovigilance (QPPV).

Key Responsibilities

• Support Individual Case Safety Report (ICSR) processing, including data entry, coding, and narrative preparation.
• Assist with case follow-up and collection of missing safety information.
• Support the assessment of seriousness, expectedness, and causality under appropriate supervision.
• Assist with safety case processing and reporting in accordance with applicable regulatory timelines.
• Maintain PV records, safety databases, and related documentation.
• Support literature screening and identification of relevant safety information.
• Assist with safety data review and signal detection activities.
• Support the preparation of PSURs/PBRERs, RMPs, and other PV documentation.
• Participate in PV compliance activities, including SOPs, CAPAs, deviations, audits, and inspections.
• Coordinate with Regulatory Affairs, Quality, and Medical Affairs on relevant PV activities.
• Participate in PV training and other departmental activities as assigned.

What You Will Gain

• Practical exposure to ICSR management and safety reporting.
• Experience in literature screening and signal detection.
• Exposure to aggregate safety reports and risk management activities.
• Understanding of PV compliance and quality systems.
• Cross-functional exposure to Regulatory Affairs, Quality, and Medical Affairs.
• Practical understanding of Saudi pharmacovigilance requirements and applicable global PV standards.
• A strong foundation for a future career in Pharmacovigilance and Drug Safety.

Qualifications & Skills

• Bachelor's degree in pharmacy or PharmD.
• Fresh graduate with a strong interest in Pharmacovigilance and Drug Safety.
• Good communication and organizational skills.
• Good command of English.
• Good knowledge of Microsoft Office.
• Strong attention to detail and analytical thinking.
• Ability to work with scientific and medical information.
• Willingness to learn and maintain confidentiality.
• Must meet Tamheer eligibility requirements.