Specialist, Global PV & Epidemiology

Boehringer Ingelheim; Athens (GA); On-site; USD 110,000 - 150,000; Full time

Job summary

Boehringer Ingelheim in the United States is seeking a Specialist, Global PV & Epidemiology to deliver quantitative pharmacovigilance analytics, regulatory reporting support, and digital initiatives that strengthen global surveillance activities.

The role supports signal detection, safety governance, and data-driven analyses, collaborating with PV teams to ensure inspection-ready documentation and compliance across GxP processes.

Qualifications

• Bachelor's degree in Life Sciences, Epidemiology, Data Science, Public Health, Statistics, or related discipline required.
• Minimum of two years’ experience in regulatory/compliance (GxP) environment.
• Strong English skills (written and oral).
• Experience with Power BI, SQL, SAS, R, Python, or equivalent analytical tools.

Responsibilities

• Performs company business in accordance with regulations and company policies.
• Immediately reports noted/observed violations to management.
• Demonstrates high ethical standards with all business contacts.
• Supports/Generates and maintains monthly quantitative signal detection and signal management workflows.
• Performs data review and triage activities for signal validation.
• Generates base data/reports for analyses (line listings, two-period comparisons).
• Collaborates with PV product teams, veterinarians, epidemiologists, and safety scientists.
• Develops and maintains standardized analytical outputs for signal governance.
• Ensures analyses are inspection-ready and documented per GxP.
• Drafts monthly Signal Evaluation Committee reports/minutes.
• Documents committee discussions, decisions, actions, outcomes.
• Coordinates committee review documentation.
• Generates final reports per governance procedures.
• Conducts batch analysis supporting Requests for PV Information (RPI).
• Extracts, analyzes, and summarizes relevant safety data from PV systems.
• Prepares clear analytical summaries and timely delivery.
• Generates and coordinates regulatory PV statements/reports for EMA, UK VMD, etc.
• Supports quality control, reconciliation, and submission-readiness.
• Maintains documentation per GxP.
• Proactively identifies automation, digitalization, and AI opportunities in PV.
• Partners with stakeholders to design, test, implement PV improvements.
• Supports development of automated analytics, dashboards, workflows.
• Contributes to AI and advanced analytics initiatives.
• Develops expertise in designated PV systems and tools.

Skills

Regulatory compliance

Data analysis

Team collaboration

Strong English communication

Education

Bachelor's degree in Life Sciences or related discipline

Tools

Power BI

SQL

SAS

R

Python

Microsoft Office

Job description

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides an opportunity for all employees to collaborate internationally, offering visibility and the opportunity to directly contribute to the company's success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Specialist, Global PV & Epidemiology is responsible for delivering quantitative pharmacovigilance analytics, regulatory reporting support, and digital initiatives that strengthen global surveillance activities. This role provides analytical expertise to support signal detection, signal validation, safety governance, regulatory compliance, and operational excellence across the Global Pharmacovigilance organization. The position holder serves as a key contributor to the evaluation and prioritization of safety observations through data-driven analyses, supports health authority reporting obligations, and drives development of automation and artificial intelligence solutions to improve efficiency and effectiveness of PV processes.

Description

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides an opportunity for all employees to collaborate internationally, offering visibility and the opportunity to directly contribute to the company's success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Specialist, Global PV & Epidemiology is responsible for delivering quantitative pharmacovigilance analytics, regulatory reporting support, and digital initiatives that strengthen global surveillance activities. This role provides analytical expertise to support signal detection, signal validation, safety governance, regulatory compliance, and operational excellence across the Global Pharmacovigilance organization. The position holder serves as a key contributor to the evaluation and prioritization of safety observations through data-driven analyses, supports health authority reporting obligations, and drives development of automation and artificial intelligence solutions to improve efficiency and effectiveness of PV processes.

Duties & Responsibilities

• Performs all company business in accordance with all regulations and company policies and procedures
• Immediately reports noted/observed violations to management
• Demonstrates high ethical and professional standards with all business contacts to maintain company's excellent reputation in the community

Quantitative Signal Analytics & Signal Management

• Supports/Generates and maintains monthly quantitative signal detection and signal management workflows
• Performs data review and triage activities to identify observations requiring advancement to signal validation
• Generates base data/reports as required for further analysis (line listings, two-period comparisons)
• Performs batch analyses and seasonality evaluations as required to support safety assessments
• Collaborates with PV product responsible persons, veterinarians, epidemiologists, and safety scientists to interpret analytical findings
• Develops and maintains standardized analytical outputs and documentation supporting signal governance activities
• Ensures analyses are inspection-ready, reproducible, and appropriately documented according to GxP

Signal Evaluation Committee Reporting

• Drafts monthly Signal Evaluation Committee meeting reports and minutes
• Documents committee discussions, decisions, actions, and outcomes
• Coordinates committee review and decision documentation
• Generates final reports in accordance with established governance procedures
• Maintains archival records supporting regulatory and inspection requirements according to GxP and GDP

Requests for PV Information Support

• Conducts batch analysis activities supporting Requests for PV Information (RPI)
• Extracts, analyzes, and summarizes relevant safety data from pharmacovigilance databases and reporting systems
• Prepares clear and accurate analytical summaries
• Ensures timely delivery of responses while maintaining data quality and compliance requirements

Regulatory Reporting & Annual Statements

• Generates and coordinates annual and periodic pharmacovigilance statements/reports required by global health authorities
• Prepares Annual Statement reports for: European Medicines Agency (EMA), Israel Ministry of Health, United Kingdom VMD, etc
• Supports quality control, reconciliation, and submission-readiness activities
• Maintains documentation and compliance records according to GxP

PV Innovation, Automation & Systems Excellence

• Proactively identifies opportunities to improve efficiency through automation, digitalization, and AI-enabled solutions
• Partners with stakeholders to design, test, and implement innovative PV process improvements
• Supports development of automated analytics, reporting tools, dashboards, and workflow solutions
• Contributes to strategic initiatives involving artificial intelligence and advanced analytics within Global PV
• Develops expertise in designated PV systems and tools

Requirements

• Bachelor's degree in Life Sciences, Epidemiology, Data Science, Public Health, Statistics, or related discipline required
• Minimum of two (2) years’ experience working in a regulatory/compliance (GxP) environment. Epidemiology, pharmacovigilance, drug safety, or related field preferred
• Strong English skills (written and oral)
• Strong working knowledge of Microsoft Office products
• Experience with Power BI, SQL, SAS, R, Python, or equivalent analytical tools
• Must have strong organizational and time management skills to work with diverse cultures and departments
• Ability to work in a team environment or experience working in a project environment
• Attention to detail quality focused and strong technical and problem-solving skills
• Experience performing quantitative analysis and/or data interpretation
• Experience working with large datasets and reporting tools
• Experience with AI, automation, workflow tools, or digital transformation initiatives
• Knowledge of adverse event signal management processes is a plus
• Experience with FDA, EMA and/or other animal health regulatory agencies is preferred
• Familiarity with MedDRA and/or VeDDRA terminology is a plus.

Eligibility Requirements

• Must be legally authorized to work in the United States without restriction
• Must be willing to take a drug test and post-offer physical (if required)
• Must be 18 years of age or older

Our Company

Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry's top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,300 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at www.boehringer-ingelheim.com.

Why Boehringer Ingelheim?

With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.

Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.

Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.

Want to learn more? Visit https://www.boehringer-ingelheim.com