In this role, one must collaborate with global clients and cross-functional teams to provide epidemiology expertise for real-world evidence (RWE) studies across the full spectrum of study designs and methodologies, spanning early clinical development through post-approval stages. Support research initiatives including, but not limited to, natural history of disease studies, external comparator studies, and comparative safety and effectiveness evaluations of drugs, biologics, and medical devices under the guidance of senior staff. Design scientifically rigorous and methodologically sound studies that align with project objectives and stakeholder requirements, including regulatory and payer expectations. Contribute to data collection strategy through input on eCRF design, feasibility assessments, and data landscape evaluations. Conduct and review analyses, interpret study findings, and support the preparation of study reports and other deliverables. Responsibilities may range from providing feasibility insights to developing study protocols and clinical study reports, while ensuring data quality, scientific integrity, and operational excellence throughout all phases of real-world studies. May also contribute to business development activities to support client retention and growth opportunities.
Key Responsibilities:
Lead the design, implementation, and execution of epidemiology and pharmacoepidemiology methodologies for real-world evidence (RWE) studies, including drug safety, comparative effectiveness, observational, and low-intervention research utilizing real-world data sources.
Provide scientific and methodological expertise to support research initiatives and strategic projects in collaboration with senior team members.
Serve as the project lead for smaller studies and work closely with senior project leaders on larger client-facing and internal projects.
Develop and author study protocols, statistical analysis plans, clinical study reports, and other research documentation, ensuring high standards of scientific quality, accuracy, and completeness.
Manage analysis and reporting deliverables, maintaining project timelines and identifying risks or issues requiring escalation when appropriate.
Review study analyses and provide epidemiological input into statistical analysis plans, analytical outputs, and interpretation of study findings.
Contribute epidemiological expertise to case report form (CRF/eCRF) design, form review, feasibility assessments, regulatory responses, presentation materials, and other ad hoc project activities.
Engage directly with clients to discuss study design, methodology, results, and project progress, with senior oversight as needed.
Identify and proactively address project, client, budgetary, and operational challenges to support successful project delivery.
Ensure efficient use of project resources and work within approved budgets while maintaining quality standards.
Drive continuous process improvement initiatives and contribute to the development and implementation of best practices across epidemiology and observational research teams.
Support business development efforts through proposal development, scientific input, and content creation for new opportunities.
Represent the organization externally through scientific conferences, professional meetings, publications, and presentations.
Oversee or conduct statistical analyses, as required, to support study objectives and deliverables.
Contribute to internal strategic initiatives aimed at enhancing scientific excellence, methodological innovation, and operational effectiveness.
Qualifications:
Education & Experience
Master's degree in Epidemiology, Pharmacoepidemiology, Public Health (with a concentration in Epidemiology), Pharmacy (with a concentration in Epidemiology), or a related scientific discipline, with a minimum of 5 years of relevant professional experience; or
PhD in Epidemiology, Pharmacoepidemiology, Public Health, Pharmacy, or a related field with at least 2 years of relevant experience.
Knowledge & Skills
Strong methodological foundation in epidemiology, pharmacoepidemiology, observational health research, and real-world evidence generation.
Demonstrated ability to design, plan, and execute observational studies evaluating comparative safety and effectiveness outcomes.
Experience developing study protocols, analysis plans, study reports, and other scientific and regulatory documentation.
Excellent written and verbal communication skills, including the ability to communicate complex scientific concepts to diverse audiences.
Strong client-facing skills with the ability to establish and maintain effective relationships in a global, matrixed environment.
Exceptional attention to detail, organizational skills, and the ability to manage multiple priorities simultaneously.
Proven ability to collaborate effectively across multidisciplinary and international teams.
Proficiency in Microsoft Word, Excel, PowerPoint, and Edge.
Ability to interpret and review outputs generated from statistical programming tools such as SAS, R, or equivalent analytical software.
Preferred Qualifications
Experience presenting research findings at scientific conferences and contributing to peer-reviewed publications.
Experience supporting business development activities, proposal preparation, and client engagement initiatives.
Knowledge of regulatory expectations and industry best practices related to real-world evidence, observational research, and pharmacoepidemiology.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.
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