Specialist, Global PV & Epidemiology

Boehringer Ingelheim; Athens (GA); Hybrid; USD 90,000 - 130,000; Full time

Job summary

Boehringer Ingelheim Animal Health USA is seeking a Specialist in Global Pharmacovigilance & Epidemiology to drive quantitative analytics, regulatory reporting support, and digital PV initiatives. The role emphasizes signal detection, governance, and data-driven safety insights across global PV operations.

The position requires a Life Sciences/epidemiology background, 2+ years in a GxP environment, and strong analytical skills with Power BI, SQL, SAS, R, or Python.

Qualifications

• Bachelor's degree in Life Sciences, Epidemiology, Data Science, Public Health, Statistics, or related discipline.
• Minimum of two years' experience in regulatory/compliance (GxP) environment.
• 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.
• Attention to detail, quality-focused and strong technical/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 or other regulatory agencies is preferred.
• Familiarity with MedDRA/VeDDRA terminology is a plus.

Responsibilities

• Performs all company business in accordance with regulations and company policies.
• Reports observed violations to management.
• Maintains ethical standards to protect the company's reputation.
• Supports/Generates monthly signal detection and signal management workflows.
• Collaborates with PV product teams, epidemiologists, and safety scientists to interpret analyses.
• Develops standardized analytical outputs supporting signal governance.
• Ensures analyses are inspection-ready and properly documented.
• Drafts monthly Signal Evaluation Committee reports and minutes.
• Documents committee decisions and outcomes; coordinates review and documentation.
• Generates final reports per governance procedures.
• Maintains archival records for regulatory and inspection requirements.
• Conducts batch analysis for Requests for PV Information (RPI).
• Extracts, analyzes, and summarizes relevant safety data from PV databases.
• Prepares concise analytical summaries and ensures timely delivery.
• Generates and coordinates PV regulatory reports and annual statements (EMA, UK, etc.).
• Supports QA, reconciliation, and submission-readiness activities.
• Maintains documentation per GxP.
• Identifies automation and AI opportunities; supports digital PV initiatives.
• Partners to design, test, and implement PV process improvements.
• Develops dashboards and workflow solutions; contributes to AI initiatives within Global PV.

Skills

English proficiency

Regulatory compliance

Organizational skills

Team collaboration

Attention to detail

Problem solving

Quantitative analysis

Education

Bachelor's degree (Life Sciences/EP/HQS)

Tools

Power BI

SQL

SAS

R

Python

Job description

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) yearsâ 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.

JOB ID

36928

Job function

Regulatory Affairs

Career level

Experienced professionals

Organization

Boehringer Ingelheim Animal Health USA

Working time

Full-Time

Job flexibility

Hybrid

Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients, and communities. All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law