Epidemiologist (real world country operations)

IQVIA LLC

Madrid

Presencial

EUR 45.000 - 70.000

Jornada completa

14 días+
Generador de candidaturas

Transforma esta oferta en una entrevista: un currículum y una carta de presentación creados pensando en lo que quiere el empleador.

Supera los filtros ATS

Descripción de la vacante

IQVIA LLC is seeking an Epidemiologist in Madrid to lead high-quality real-world evidence studies. The role involves managing epidemiology for studies throughout the product lifecycle, from development to post-approval.

Qualified candidates should have a Master's or Ph.D. in epidemiology or a related field, and strong project management skills. The position offers an engaging opportunity to contribute to innovative health solutions globally.

Formación

  • 5 years relevant experience for Master's or 2 years for Ph.D.
  • Ability to design and conduct observational studies.
  • Excellent oral and written communication skills in English.

Responsabilidades

  • Lead implementation of epidemiology methods in studies.
  • Author protocols and ensuring quality delivery.
  • Support client interactions and communications.

Conocimientos

Epidemiology methods
Statistical analysis
Medical writing
Project management
Proficiency in Word, Excel, PowerPoint

Educación

Master's Degree in epidemiology or related field
Ph.D. in relevant scientific field

Herramientas

SAS
R

Descripción del empleo

## Epidemiologist (real world country operations)Applylocations: Madrid, Spaintime type: Full timeposted on: Posted 8 Days Agojob requisition id: R1541665We 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.**Essential Functions:*** 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.**Qualifications:*** 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.
Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra y suelta tu archivo aquí
Similar jobs

Puestos de trabajo similares que vale la pena comparar

Associate Director, Biostatistics
Associate Director, Biostatistics

Iqvia • Madrid

Presencial
EUR 90.000 - 120.000
Pharmaceutical Market Research Analyst (French-speaker)
Pharmaceutical Market Research Analyst (French-speaker)

IQVIA • Madrid

Presencial
EUR 35.000 - 48.000
Jr Healthcare Data Coding (Pharma) Fixed-Term
Jr Healthcare Data Coding (Pharma) Fixed-Term

IQVIA LLC • Madrid

Presencial
EUR 30.000 - 40.000
Senior Global Trial Manager
Senior Global Trial Manager

IQVIA • Barcelona

Presencial
EUR 90.000 - 120.000
Associate Medical Director- Neurology
Associate Medical Director- Neurology

IQVIA • Madrid

Presencial
EUR 120.000 - 180.000
Pharmaceutical Market Research Analyst (French-speaker)
Pharmaceutical Market Research Analyst (French-speaker)

IQVIA Argentina • Madrid

Presencial
EUR 24.000 - 32.000
Senior Clinical Research Associate 1 - Sponsor dedicated
Senior Clinical Research Associate 1 - Sponsor dedicated

3M HEALTHCARE • Barcelona

Presencial
EUR 42.000 - 64.000
Mobile phone included
Excellent benefits package
Pharmacy Graduates - (French Speaker)
Pharmacy Graduates - (French Speaker)

IQVIA • Madrid

Presencial
EUR 22.000 - 32.000
Consultant – Global Advisory Services
Consultant – Global Advisory Services

IQVIA Argentina • Madrid

Híbrido
EUR 70.000 - 110.000
Senior Global Trial Manager
Senior Global Trial Manager

IQVIA Argentina • Madrid

Presencial
EUR 90.000 - 130.000