Real World Evidence Analyst
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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Real World Evidence Analyst
Description du poste
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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