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Global Real World Evidence Associate Director
vor 2 Wochen
Over 500 Million That’s the number of real world patient records that are used to help reimagine how integrated evidence generation will transform healthcare decision making.
As our Real World Evidence Associate Director, you will enable cross-functional teams in becoming leaders in utilization and generation of Real World Evidence (RWE) as part of integrated evidence in innovative and advanced ways. You will focus on priority disease areas and gaps, be responsible for the development of an impactful and scientifically robust RWE strategy with a focus on prospective studies and retrospective clinically-oriented studies, and innovative trial designs.
Your responsibilities will include, but are not limited to:
- Ensure a broad understanding of the value and impact of RWE to the product value demonstration both globally and locally. Lead and ensure innovative study designs with best-in-class integrated evidence planning and creation with Global Drug Development (GDD), to maximize value of key development projects, products, and businesses in key geographies.
- Utilize a decision matrix to determine with Medical Affairs / Patient Access / Safety / Product teams the most suitable source of RWD and RWE generation approach that meets prioritized evidence needs. Where secondary data is not available to generate fit-for-purpose evidence recommend the most appropriate prospective data collection study design and analysis that achieves the objectives. Provides input and supports to develop high quality functional and cross-functional evidence generation plans.
- Implement and ensure uniform excellence within franchise.
- Lead innovation pilots that can support to overcome key challenges in drug development using RWD or enable to provide meaningful RWE in support of regulatory decision making (e.g. label changes, new indications).
**Commitment to Diversity & Inclusion**:
- Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._
**Minimum requirements**
- 5 years relevant experience acquired at pharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies
- Deep understanding of Medical Affairs, Market Access/ HEOR, Safety or related disciplines to generate value evidence from retrospective and prospective studies.
- Very strong understanding of drug development and commercial disciplines, proven ability to identify key evidence needs for
- Considerable experience in planning, creation, and analysis of real-world data, from both prospective and retrospective studies with a proven success record in this field
- Experienced and with a strong knowledge of research methodology and statistical methods in the field of prospective clinical data analysis
- Considerable experience in collaborating with quantitative scientists and analysts
**Division**
PHARMA
**Business Unit**
GLOBAL MEDICAL AFFAIRS
**Country**
Switzerland
**Work Location**
Basel
**Company/Legal Entity**
Novartis Pharma AG
**Alternative Country 1**
USA
**Functional Area**
Research & Development
**Job Type**
Full Time
**Employment Type**
Regular
**Shift Work**
No
**Early Talent**
No
