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Real World Evidence Analyst

Oeiras, Portugal Full time R1436966

Oeiras, Portugal| Portugal

  • Full Time
  • Level: Entry-level, Mid-level, Senior-level

Build a rewarding career in life sciences consulting and forge your own path. Partner with collaborative teams and leaders across unique projects and geographies, delivering innovative solutions to the most complex healthcare problems along the way. Working at IQVIA means changing outcomes for patients one data set, product offering and innovative solution at a time.

As a Consultant at IQVIA, you'll have the opportunity to grow your career and explore opportunities in brand and integrated research solutions, go-to-market strategy, commercial excellence, real world data, financial investor consulting and more.

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Success Profile

What makes a Consultant at IQVIA successful? Check out the top traits we’re looking for and see if you have the right mix.

  • ACHIEVER
  • ADAPTABLE
  • COMMUNICATOR
  • STRATEGIC
  • CRITICAL-THINKER
  • DETAIL-ORIENTED

What you can expect

Professional Development

Environments that advance your skillset

Highly Specialized

Work in distinctive areas of expertise

Growth Potential

Clear pathways to success

Collaboration

Teams that work together to achieve common goals

Innovative Projects

Projects that solve complex problems in new ways

Best-in-Class Training

Programs to help you build knowledge and gain skills

I joined IQVIA after graduating from university and am grateful for the fantastic opportunities I've been able to pursue over the last four years. I've had the chance to work with inspiring managers who have supported me with both professional and personal development.

Arthur

Consultant, Financial Institutions

I simultaneously work on a number of customer-commissioned projects in multiple therapeutic areas using various primary research methodologies. This variety is what makes my role so interesting. It allows me to learn from my colleagues and customers alike and helps me to understand how the work we do supports the improvement of patient care.

Julia

Senior Consultant, Brand and Integrated Research Solutions

IQVIA has given me the opportunity to gain a broad range of skills and experience across multiple disease areas and at different stages of the product lifecycle. This has supported my career development and accelerated my growth. If you enjoy learning new things and working on global projects, you will definitely enjoy working at IQVIA.

Kevin

Consultant, Brand and Integrated Research Solutions​

One of the things I like most about working at IQVIA is the supportive environment that helps you achieve your full potential.

Ana

Consultant, Financial Institutions

Working in healthcare consulting is inspiring! I am glad to be part of a close community that brings together diverse experiences and critical thinkers to help our customers move treatments forward that can change patients’ lives.

Jose

Principal, Consulting Services

Real World Evidence Analyst

Oeiras, Portugal| Portugal R1436966
Apply Now

Job Description

With approximately 85,000 employees in more than 100 countries, IQVIA is in a truly unique position to be able to support companies seeking to improve real-world patient outcomes and enhanced clinical trial outsourcing through treatment innovations, care provision, and access. With a broad range of healthcare information, technology, and service offerings, IQVIA provides solutions that span clinical to commercial, bringing clients an exceptional opportunity to realize the full potential of innovations and advance healthcare outcomes.

Role Purpose

As an Analyst within the Real World Evidence Department, you will have a key role in supporting the management of clinical dossiers. You are expected to be capable of working on different projects for different clients in the Portuguese market, so a flexible, enthusiastic, and professional approach is essential.

General Responsibilities

  • Support the health technology assessment (HTA) submission and reimbursement processes, including the preparation of Added Therapeutic Value dossiers
  • Conduct literature reviews and evidence synthesis to support clinical dossiers.
  • Support the preparation and submission of clinical trial applications and other regulatory documents.
  • Collaborate with clinical teams to ensure the accuracy and completeness of clinical data.
  • Assist in the organization and execution of Advisory Boards and consultations with Key Opinion Leaders (KOLs).
  • Contribute to the preparation, execution, and follow-up of client projects.

Qualifications

  • Degree in life sciences, pharmacy, nursing, or a related field.
  • A postgraduate degree in clinical research, pharmacy, biostatistics, epidemiology, healthcare policy, or another healthcare-related discipline.
  • Prior experience in market access will be a plus
  • Prior experience in health technology assessment will be a plus.
  • Strong understanding of clinical research methodologies of the Portuguese health care system.
  • Previous work experience in clinical or outcomes research, real-world evidence, or evidence generation.
  • Proficiency in Portuguese and English (both written and spoken).
  • Strong communication skills.
  • Excellent execution skills, consistently meeting deadlines.
  • Keenness to learn and commitment to a rapid development curve.
  • Self-driven approach and ability to work in a team.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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