Safety Database Associate

Recordati; Turbigo; In loco; EUR 32.400 - 39.600; Tempo pieno

Descrizione del lavoro

Recordati is looking for a Safety Database Associate in Turbigo, Italy to help maintain and implement systems for Pharmacovigilance activities. The role involves configuring databases, ensuring compliance with legislation, and providing user support.

Candidates should have a scientific or IT degree, along with experience in a pharmaceutical environment. Knowledge of pharmacovigilance and familiarity with systems like Oracle Argus is a plus. Starting salary is 36,000€ gross annually.

Competenze

• At least 6 months’ experience in a similar role in a pharmaceutical company.
• Basic knowledge of pharmacovigilance requirements/obligations.
• Familiarity with CSV/Data Integrity knowledge.

Mansioni

• Configure databases/tools based on new company requirements.
• Ensure system updates comply with legislation.
• Provide user support and training for PV systems.
• Support validation activities including documentation preparation.
• Prepare relevant SOPs and WIs.
• Implement new system functionalities.

Conoscenze

Pharmacovigilance knowledge

Problem-solving skills

Teamwork

Formazione

Scientific/IT degree

Strumenti

Oracle Argus

Qdocs

Veeva

Descrizione del lavoro

Job Purpose

We are looking for a Safety Database Associate to support the team in the maintenance and implementation of all the systems and tools used for the management of the Pharmacovigilance activities.

Key Responsibilities

• Databases/tools configuration based on new company requirements.
• System updates to be always in compliance with current legislation.
• Users support and training for the use of the PV systems; interaction with the concerned internal departments, Affiliates and Providers.
• Support the validation activities (such as documents preparation, validation tests executions, maintenance of documentation as required by SOPs/WIs and standards).
• Preparation of the relevant SOPs and WIs.
• New system functionalities implementation.

Required Education

Scientific/IT degree.

Required Skills And Experience

At least 6 months’ experience in a similar role in a pharmaceutical company or at least basic knowledge of pharmacovigilance requirements/obligations are required. Familiar to CSV/Data Integrity knowledge.

Technical Competencies

Nice to have: good knowledge of Pharmacovigilance Safety Databases (e.g. Oracle Argus); familiarity with Qdocs or comparable systems (such as Veeva).

Required Behaviours And Competencies

Able to work in team and have problem‑solving skills; timely management and meeting deadlines.

Required Languages

Good knowledge (written and oral) of English is required. Further knowledge of languages is well recognised.

Salary

Gross Annual Salary starting from: 36,000€.

Equal Employment Opportunity Statement

We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.