Epidemiologist (Senior Research Associate) - Evidera

Position Overview

• Location Type: Office
• Job Type: Full time
• Work Schedule: Standard (Mon-Fri)
• Team: PPD Evidera Real-World Data & Scientific Solutions

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Team Overview: Evidera is a business within Pharmaceutical Product Development, LLC (PPD), a leading global contract research organization (CRO). We provide integrated scientific expertise and global operational capabilities to help clients generate the evidence needed to optimize the market access and commercial potential of products. The Evidera Real-World Data & Scientific Solutions team supports pharmaceutical and biotechnology companies throughout the product lifecycle, from early pre-launch planning to launch and post-marketing management. Our focus is on helping our clients build economic and epidemiological evidence to demonstrate and support the value of their products, through analysis of large health administrative databases (e.g., medical claims, electronic health records, registries, etc.).

Position Overview: The Epidemiologist, Senior Research Associate will bear scientific responsibility for the design and implementation of retrospective observational studies using secondary data sources, bringing project deliverables to near completion with the oversight of more senior staff. Real-world data used will range from EMR, claims, and registries worldwide, but a focus on clinical registries in Europe, to address pharmacoepidemiological research questions around the effectiveness and safety of drugs. Solid communication and interpersonal skills will be required to develop and sustain positive rapport with the team and external contacts including clients and other stakeholders such as data vendors and registry holders.

Responsibilities

• Provides scientific guidance and consultation on scientific and logistical considerations of study design and conduct.
• Drafts or reviews initial drafts of project deliverables (e.g., protocols, analysis plans, reports) before final senior review.
• In some client engagements, serves as Principal Investigator, with final responsibilities for project budget, deliverables, and timelines.
• Contributes to the growth of Evidera through business development activities, including proposal development, participation in the sales cycle, conference attendance, and presentations.
• Supports other organizational activities as needed (e.g., staff; closely collaborate with other business units; contribute to development of training materials and process improvements).
• Interacts directly with sponsors and external stakeholders.

Education, Professional Skills & Experience

• Master’s or PhD in Epidemiology or Public Health.
• A minimum of 3 years’ pharmaceutical experience, including experience as a consultant with a pharmacoepidemiology or health economics and outcomes research (HEOR) focus.
• Applied experience in quantitative methods in epidemiology/pharmacoepidemiology with a focus on data analysis using real-world observational data (e.g., claims data, electronic medical records).
• Experience working with clinical registries and data harmonization.