Madrid, Community of Madrid, Spain · On-site
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Madrid, Community of Madrid, Spain · Remote Solely
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Madrid, Community of Madrid, Spain · On-site
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Madrid, Community of Madrid, Spain · On-site
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Madrid, Community of Madrid, Spain · Remote Solely
$40/hr–$40/hr
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Madrid, Community of Madrid, Spain · Hybrid
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Madrid, Community of Madrid, Spain · Hybrid
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Madrid, Community of Madrid, Spain · Hybrid
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Madrid, Community of Madrid, Spain · On-site
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Madrid, Community of Madrid, Spain · Remote OK
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Madrid, Community of Madrid, Spain · On-site
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Madrid, Community of Madrid, Spain · On-site
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Madrid, Community of Madrid, Spain · Remote OK
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Madrid, Community of Madrid, Spain · On-site
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Madrid, Community of Madrid, Spain · On-site
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Madrid, Community of Madrid, Spain · Remote OK
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Lead the design and implementation of epidemiology and pharmacoepidemiology methods for real-world evidence studies across the product lifecycle. Author protocols and reports while partnering with global clients and cross-functional teams to ensure high-quality delivery.
Requires a Master's degree in epidemiology or a related field with 5 years of experience, or a PhD with 2 years of experience. Must possess strong methodological training in observational health research and proficiency in English communication.
We are seeking a dedicated Epidemiology professional to support the design and delivery of high-quality real-world evidence studies in a global, cross-functional environment.
The role would entail to partner with global clients and cross-functional teams to lead epidemiology for real-world studies across the full product lifecycle, from early clinical development through post-approval. Responsibilities range from feasibility assessments to developing protocols and clinical study reports, with opportunities to support business development and strengthen client relationships.
Lead the design and implementation of epidemiology and pharmacoepidemiology methods in real-world studies, including drug safety, effectiveness, and observational research.
Translate research objectives into fit-for-purpose study designs (e.g., cohort, case-control, cross-sectional, pragmatic, survey-based), defining endpoints, populations, and analytic strategies.
Serve as project lead on smaller studies or support larger client-facing and internal projects.
Author protocols, reports, and study documents, ensuring quality, completeness, and timely delivery.
Provide epidemiological input into statistical analysis plans and review analysis outputs.
Contribute to CRF/eCRF design, form reviews, and other project deliverables (e.g., regulatory responses, presentations).
Support client interactions and communications, with senior oversight as needed.
Identify and escalate project, budget, or client-related risks and issues.
Ensure work is delivered within agreed budgets and timelines.
Contribute to process improvements and the development of best practices.
Support business development activities, including proposal content for smaller projects.
Represent the organization externally (e.g., conferences, presentations) as appropriate.
Oversee or conduct statistical analyses when required.
Contribute to proposal development and internal initiatives in epidemiology and observational research.
Master's Degree Graduate education in epidemiology, pharmacoepidemiology, public health with concentration in epidemiology, pharmacy with concentration in epidemiology or relevant scientific field and 5 years relevant experience Req or Ph.D. with 2 years relevant experience is preferred.
Sound methodological training in epidemiology, pharmacoepidemiology, public health with concentration in epidemiology, pharmacy with concentration in epidemiology or related area relevant to observational health research.
Ability to design, plan and conduct observational studies of comparative effectiveness and safety.
Excellent oral and written communication skills in English, medical writing experience beneficial.
Ability to establish and maintain effective working relationships with coworkers, managers and clients in a global and matrixed environment.
Exceptional attention to detail and the ability to effectively prioritize and manage multiple tasks.
Ability to work collaboratively with diverse team members.
Must be proficient in Word, Excel, PowerPoint and Edge. Ability to read outputs from SAS, R or other programming languages.
Must be highly organized and self-motivated with ability to determine and meet objectives.
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.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
There are currently 263 open science & research positions in Madrid, Spain listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include IQVIA, CEU Universities, Indra Group USA, ROVI Pharmaceutical Company, ACCIONA, among others. Browse the listings above to see every active employer.
Yes — 105 of the 263 open science & research positions offer remote or hybrid work (24 remote, 81 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
