Epidemiologist

IQVIA Argentina; Cataluña; Presencial; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

IQVIA is seeking an experienced epidemiologist to design and execute real-world evidence studies across drug, device and biologic portfolios. You will lead observational research, contribute to protocols, and coordinate with global teams to deliver high-quality analyses and reports.

The role requires strong expertise in pharmacoepidemiology, study design, and statistical analysis, with excellent communication skills for stakeholders. Office-based in a global environment.

Formación

• Master's or PhD with relevant professional experience in epidemiology or pharmacoepidemiology.
• Experience designing observational studies and reporting study results.
• Strong communication skills for diverse audiences.

Responsabilidades

• Lead design and execution of epidemiology methods for real-world studies.
• Act as project lead for smaller studies and support larger client projects.
• Develop study protocols, SAPs, and clinical study reports with high scientific standards.
• Manage analyses, timelines, and risks; ensure data quality and integrity.
• Engage with clients to discuss design, results, and progress.

Conocimientos

Epidemiology

Pharmacoepidemiology

Study design

Statistical analysis

Client communication

Regulatory knowledge

Cross-functional collaboration

MS Word/Excel/PowerPoint

Educación

Master's in Epidemiology

PhD in Epidemiology/Pharmacoepidemiology

Herramientas

SAS

R

Excel

Descripción del empleo

Barcelona, Spain | Full time | Office-based | R1553653

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.

Where you'll work

Office-based

You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.

"I like that we're different. I like that we're a unique organization unlike any other. I like to think of us as the intelligence company for life sciences and healthcare. I do believe there's nothing else like this organization in the world. So if you like something that's different and interesting, you're going to like IQVIA. If you like an organization that has a variety of opportunities, from IT to big data to AI to finance to HR, there are so many opportunities to have an impact."

"The culture in IQVIA is to be constantly looking at how we can do things better to help our customers, to bring life-changing medicines to patients and also to be a part in designing and developing and implementing these solutions. And so I think it's a great place to join because there is that organizational focus and commitment in driving forward the innovation and just the ability, I think, to work with cross-functional teams who are all excited to be working in these areas. It's a fantastic opportunity."

"First of all, we are humans, we have some moments in our lives that are so very important and we need to respect. And something I also always love about IQVIA was that my leaders and people with which I have been working, they always respected a lot as well our personal lives. I never miss a parents' meeting of my kids, and this is something that we shouldn't be giving for granted."

Senior Director Global Site Activation

"I like that we're different. I like that we're a unique organization unlike any other. I like to think of us as the intelligence company for life sciences and healthcare. I do believe there's nothing else like this organization in the world. So if you like something that's different and interesting, you're going to like IQVIA. If you like an organization that has a variety of opportunities, from IT to big data to AI to finance to HR, there are so many opportunities to have an impact."

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.