Pharmacovigilance Systems Programmer

JR United Kingdom; Hart; Hybrid; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Pharmacovigilance Systems Programmer to enhance their medical services systems. This hybrid role involves managing database transitions, ensuring regulatory compliance, and optimizing safety databases. The ideal candidate will possess strong programming skills, particularly in SQL, and a solid understanding of pharmacovigilance processes. Join a dynamic team where your expertise will contribute to improving patient safety and compliance across the EU and UK markets. This is an exciting opportunity to be part of a forward-thinking organization dedicated to excellence in the pharmaceutical industry.

Qualifications

• Experience in pharmacovigilance systems programming and database management.
• Strong coding skills, particularly in SQL, for data manipulation.

Responsibilities

• Manage the transition of the Argus safety database to Halo PV.
• Develop and optimize SQL queries for pharmacovigilance systems.
• Ensure compliance with Good Pharmacovigilance Practices.

Skills

SQL

Pharmacovigilance processes

Data integrity

Analytical skills

Problem-solving

Tools

Argus

Veeva

HaloPV

Job description

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Pharmacovigilance Systems Programmer, Hartley Wintney

Client: TMC Pharma Services Ltd

Location: Hartley Wintney, United Kingdom

Job Category: Other

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EU work permit required: Yes

Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

Job Description:

Reporting directly to the Head of PV and Medical Director, we are seeking a skilled Pharmacovigilance Systems Programmer experienced in PV and medical systems (e.g., Argus, Veeva, HaloPV, etc.) with expertise in coding (e.g., SQL), systems programming, configurations, validation, report and dashboard development, ideally with a background in pharmacovigilance (PV). The role involves supporting the transition, setup, and maintenance of safety databases and medical services systems at TMC. The ideal candidate will have experience with industry-standard databases, programming skills, and knowledge of pharmacovigilance processes in the EU, US, and/or UK markets. They will play a key role in ensuring seamless database migrations, implementations, and customizations for client-specific requirements, ensuring compliance with regulatory standards.

Note: THIS ROLE IS HYBRID, BASED IN HARTLEY WINTNEY, HAMPSHIRE, UK.

Key Responsibilities

• Manage the transition and setup of the existing Argus safety database to Halo PV, ensuring regulatory compliance.
• Develop, maintain, and optimize SQL queries for pharmacovigilance and medical information systems.
• Configure and maintain Veeva for medical services (Veeva MedComm module and PromoMats module), ensuring efficient data capture, process management, and reporting.
• Collaborate with pharmacovigilance and IT teams to enhance system functionality and user experience.
• Ensure data integrity, security, and compliance with Good Pharmacovigilance Practices (GVP) and other relevant guidelines.
• Support automation, troubleshooting, and performance optimization of safety and medical databases.
• Assist in validation, documentation, creation of work instructions, and user training related to database implementation, integration, transitions, and management.

Key Skills

• Strong numeracy skills, comfortable working with data.
• Knowledge of the pharmaceutical development lifecycle and environment is advantageous.
• Excellent analytical skills and a problem-solving mindset.