Safety Data Management Specialist with French

TN Poland; Warszawa; On-site; EUR 40,000 - 80,000; Full time

Job summary

Join a global leader in the biopharmaceutical industry as a Safety Data Management Specialist in Warsaw. This role offers an exciting opportunity to work within a dynamic safety organization, engaging with local stakeholders in pharmacovigilance. You will be responsible for reviewing and documenting case-related information, ensuring data accuracy, and coordinating safety data collection efforts. The position promises a competitive salary, a comprehensive benefits package, and a supportive international culture that fosters professional growth. If you are fluent in English and French and possess a Master's degree in a relevant field, this could be the perfect opportunity for you.

Benefits

Medical care

Insurance

Multisport

Development opportunities

Qualifications

• Fluency in English and French is mandatory.
• Master's degree in pharmacy, biology, or related fields required.
• Experience in pharmacovigilance is advantageous.

Responsibilities

• Review and document case-related information accurately.
• Coordinate with stakeholders for safety data collection.
• Report to the Drug Safety Team Manager.

Skills

Fluency in English

Fluency in French

Problem-solving skills

Decision-making ability

Education

Master's degree in pharmacy

Master's degree in biology

Master's degree in biotechnology

Tools

Relational databases

Computer literacy

Job description

Safety Data Management Specialist with French, Warsaw

Client:

Location:

Warsaw, Poland

Job Category:

Other

EU work permit required:

Yes

Job Reference:

24146b7721f5

Job Views:

2

Posted:

02.05.2025

Expiry Date:

16.06.2025

Job Description:

Pfizer, a global leader in the biopharmaceutical industry, is seeking qualified candidates for the regional safety hub in Warsaw. Join the EUAfME Platform Team to be part of an evolving safety organization working across the region with local stakeholders in pharmacovigilance.

Responsibilities:

• Review, verify, process, and document case-related information, including event terms, validity, seriousness, and timelines.
• Assess cases to determine appropriate processing workflows and escalate complex issues.
• Write and edit case narratives, perform follow-up actions, and ensure data accuracy and compliance.
• Coordinate with stakeholders regarding safety data collection and reconciliation.
• Report to the Drug Safety Team Manager.

Qualifications:

• Fluency in English and French (spoken and written).
• Master's degree in pharmacy, biology, biotechnology, or related fields.
• Experience in pharmacovigilance, data management, or medical writing is advantageous but not mandatory.
• Proficiency with relational databases and computer literacy.
• Ability to solve routine problems, make decisions, and work under supervision in a matrix organization.

What We Offer:

• Employment contract with Pfizer.
• Competitive salary and bonus opportunities.
• Benefits package including medical care, insurance, Multisport, and more.
• International, supportive culture with development opportunities.

Please apply in English only!