Senior Consultant - Health Technology Assessment (Portugal, Hybrid)
iqvia · Porto Salvo
Job description
About the role
This is a management role within the IQVIA Global Health Economics and HTA team, focused on health technology assessment (HTA) and on shaping the team's UK HTA offerings. The role supports clients in designing evidence generation and dissemination strategies that meet HTA requirements and optimise market access. It is based in Portugal (the listing says Spain, Greece, Portugal or South Africa) with flexibility between office and home working.
Key responsibilities
- Shape and lead the team and its offerings, working with senior leadership and global centres of excellence
- Manage business development, client relationships and project scope, with senior oversight
- Manage HTA project strategy, especially UK HTA processes and requirements, and develop risk mitigation strategies
- Lead the project delivery team on dossier development, submission support for UK HTA agencies, early scientific advice and other strategic HTA offerings, and contribute to multi-country and global projects
- Mediate, negotiate and solve problems within and outside the project team, and mentor junior team members
- Work with technical consultants, Market Access, Patient-Centered Solutions, database studies and local teams, and liaise with pharmaceutical, biotechnology and medical device clients
- Support or lead thought leadership on HTA, such as conference abstracts, white papers and peer-reviewed publications, and guide interns on HTA thesis topics
- Provide line management depending on interest
Required profile
- Postgraduate degree or higher in a relevant discipline (HTA, health economics, epidemiology, biostatistics, public health, medicine, pharmacy, etc.) and at least 4 years of relevant experience preparing HTA-aligned evidence submissions in the UK and/or Europe, including appraisal and negotiation
- Experience with UK HTA submissions and early scientific advice; multi-country HTA experience highly desirable
- Good understanding of the pharmaceutical industry structure and a network of HEOR contacts highly desirable
- Proven consultancy skills and experience in a consultancy environment highly desirable
- Fluent English; applications must be submitted in English
Required skills
- Project management and managing multidisciplinary teams
- Understanding of clinical trial design, statistical methods and evidence synthesis
- Biostatistics and health economic modelling, and statistical software such as STATA and R, desirable but not essential
What we offer
- A structured onboarding programme during the first three months
- Numerous training opportunities, including external trainings aligned with business and team objectives
Questions fréquentes
Why are you reporting this job?
Explore further
Salaries, guides and searches in Portugal.
Salaries by job title
Apply in 30 seconds
Enter your email to apply. An account will be created automatically.
By continuing, you accept our terms of use.
Already have an account? Login
A question about this job?
Ask it here: you will get the full job summary by e-mail, right away.
Published 7 hours ago
Expires 1 month from now
4 views · 0 interested
Boost your chances
Upload your CV — we will match you with relevant openings.
Analyzing your CV...
iqvia
Porto Salvo
Related job offers
-
Clinical Scientist - Cronos (Home-Based, Portugal)
iqvia Porto Salvo -
Epidemiologist - Real-World Evidence Studies
iqvia Porto Salvo -
Senior Manager, Trial Delivery Leader
jj Porto Salvo -
Clinical Research Associate 2 - Portugal
iqvia Lisbon -
Independent Rater - Clinical Trials (Portuguese Speaker)
iqvia Lisbon