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We are currently looking to recruit an experienced Director RWD Strategy - Europe to join us in select European locations
Picture Yourself At Parexel:
The Director, RWD Strategy – Europe is responsible for identifying and implementing innovative access to real-world scientific data (RWD) within the region of both broad and deep patient clinical domains. This includes being proactive and determining the best methods for partnering with health systems, data vendors, national/regional patient registries, disease-specific registries and other novel sources of real-world scientific data. This is an advanced role that requires hands-on RWD experience and leadership competencies, accountability, relationship management skills and business acumen. Individuals must ensure that the application of RWD for a given solution is fit-for-purpose and is used in a manner compliant with the data use agreement and applicable law.
The Director, RWD Strategy – Europe will be enthusiastic and hands-on to develop high quality proposal material, engage with clients during bid proposals meetings, partner with multiple data partners across the region, and create RWD strategies for the region. This role offers keen insights into innovative methodologies such as AI use in RWE, PASS and therapy area applications using RWD as well as specific expertise in EMA regulatory guidance to chart a successful path forward for generating evidence from RWD.
What You'll Do At Parexel:
Proposal Development | Science | Data Insights | Vendor Management:
Proposal Development and Client Bid Proposals
1. Responsible for hands-on development of high-quality, client-ready RWD Strategy-related materials for client opportunities via PPT and Word documents
2. Attend and represent RWD Strategy for Europe opportunities with clients
3. Identify opportunities where RWD will be a value-add and positioning RWD Strategies to deliver winning solutions
Scientific and Real-World Data Asset Access
4. Responsible for the execution of a global RWD acquisition strategy within the region
5. Solution for gaps in Parexel’s scientific and real-world data coverage. Identify, assess, and recommend options to expand access to RWD and scientific data to fill gaps in Parexel’s coverage within the region
6. Perform return-on-investment assessments that inform decision-making on whether to strategically partner with select data providers
7. Operate governance frameworks for regional RWD partners and suppliers
8. Responsible for specifications being up-to-date in the data catalog (e.g., new functionality), as well as training and use across business partners
9. Ensure that data access and use is fully operational
10. Evolve regional data acquisition with business partner strategy and needs
11. Monitor KPIs used to ensure impactful use of data. Remediate to deliver return-on-investment as required
Vendor / Provider management
12. Monitor partner capabilities and services, making recommendations on ways in which the partnership can be strengthened (e.g., improve direct access, feasibility turnaround)
13. Work with Procurement/LRM to establish/manage qualification, due diligence and contracting
14. Follow up on how projects are going and what can be improved in terms of the PXL-partner relationship
15. Suppliers at minimum to include EMR / EHR; claims; pharmacy; lab, specialty data such as biomarker, genetic, and imaging; registries; clinical outcomes assessments, investigators or expert networks and similar sources of patient data beyond randomized clinical trial data
Infrastructure & Platform Design
16. Partners with technology teams to ensure region-specific requirements for system architecture are met
17. Contribute to descriptive content that can be used in capability presentations, proposals, protocols/SAPs, study reports, etc.
18. Identifies and surfaces regional observations and trends that can inform further growth
Relationship Management
19. Develop and maintain working relationships with SDO core solutions teams and functional teams, Parexel business partners, clients and vendors, providers; at minimum, Legal and Risk Management, Procurement, Data Privacy, Project team personnel
20. Maintaining relationships with regulatory bodies, organizations, and staying up to date on the current RWD landscape in Europe
What We’re Looking For:
10+ years of industry experience (CRO/Pharma/Data Vendor) with the ability to demonstrate the following:
21. In depth understanding of the clinical research process and business, medicines and medical device development, healthcare market and related sectors
22. Broad cross-functional experience in the healthcare, scientific and real-world data environment
23. Experience with major patient data models (e.g. CDISC, OMOP, LOINC, FHIR, MEDra, SnoMED etc.)
24. Demonstrated ability to apply scientific or real-world data solutions to address clinical or commercial questions and needs
25. Experienced in budgets and cost evaluation of RWD based solutions
26. Understanding of project management principles
27. Master’s degree in biomedical informatics, public health, data science, life sciences or related field
28. Advanced degree (or equivalent experience) in biomedical informatics, public health, data science, life sciences or related field desired
29. Effective translation of strategy into executable plans
30. Leadership skills in an evolving environment – change management
31. Excellent oral and written communication skills
32. Excellent customer focus (internal and external)
33. Experienced in establishing meaningful external partnerships & collaborations with health systems, vendor companies, and individual contributors within the region
34. Ability to manage multiple projects and priorities
35. Ability to identify where regulated requirements apply
36. Technical skills preparing and processing RWD for application and analysis