At a Glance
- Tasks: Lead international real-world evidence initiatives and collaborate with cross-functional teams.
- Company: Join AbbVie, a leader in innovative medicines making a real impact on health.
- Benefits: Enjoy competitive pay, comprehensive benefits, and opportunities for professional growth.
- Other info: Dynamic work environment with a commitment to diversity and inclusion.
- Why this job: Be at the forefront of healthcare innovation and contribute to meaningful change.
- Qualifications: Advanced degree and 8-10 years of experience in real-world evidence and outcomes research.
The predicted salary is between 63000 - 77000 £ per year.
About AbbVie: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.
The International RWE Lead will serve as the primary interface for the international real-world evidence (RWE) community, linking area and affiliate stakeholders to the Medical Affairs + Health Impact (MHI) RWE Center of Excellence (CoE), and cross-functional research functions including but not limited to International Market Access and Pricing (IMAP), Epidemiology (EPI), Data Science & Statistics (DSS) and R&D Data Convergence. This role will enable the generation of fit-for-purpose RWE via use of optimal RWD and methodologies across international affiliates and act as a crucial nexus across AbbVie's RWE capabilities. A key responsibility will be developing appropriate forums and ways of working across the International community and cross-functional research functions for enhancing strategic RWE planning and generation, while actively participating in Area Evidence Teams.
Responsibilities:
- Serve as the RWE subject matter expert within the assigned region and/or therapeutic areas, championing the understanding and use of primary and secondary RWD and supporting affiliates/areas in the translation of evidence gaps to robust and tangible study design through methodological input.
- Work with the Value and Evidence RWE pillars and cross-functional research functions to coordinate optimal expertise based on specific International Area & Affiliate research needs.
- Contribute to building Global-International and affiliate-area RWE networks, highlighting available expertise & resources and delivering RWD/E input and training.
- Co-lead the Asset RWE Community in partnership with International Medical and Market Access including defining the specific needs, format and membership for each asset.
- Where necessary, support evidence planning to focus on optimal real world study design to meet strategic cross-functional needs.
- In collaboration with Global RWE Innovative Real-World Data and Policy, stay current with evolving RWE guidelines, innovations, emerging trends and best practices.
- Represent AbbVie on relevant external consortia and partner with local stakeholders to drive innovative use of RWD.
- Serve as a member of the Area Review Committee (ARC), Area Evidence Teams and priority Local Evidence Teams, as needed, providing input into International evidence plans.
- Engage with external vendors/data owners to identify opportunities for smart evidence generation and represent AbbVie at external and internal International RWE meetings, as needed.
- Support evolution of International knowledge and use of RWD sources, in partnership with the V&E RWE CoE’s and cross-functional research functions.
- Represent International RWE in internal RWD/E and evidence generation workstreams, as needed.
- Actively engage with the broader International and US RWE lead community to share ideas, learnings and best practices to evolve RWE customer excellence.
Qualifications:
- Education: Advanced degree in public health, health economics, outcomes research, epidemiology, biostats, or another relevant field.
- RWE experience: Minimum of 8-10 years hands-on experience in international RWE, outcomes research, etc. within the pharmaceutical, academia, or consultancy sectors to support market access, medical and commercial evidence needs.
- Demonstrated experience with study/protocol design to meet strategic needs using a range of RWD sources.
- Deep understanding of OUS RWD/E landscape in at least 1 region (Europe, JAPAC, Canada, LATAM).
- Analytics experience desirable but not essential.
- Integrated evidence planning experience: Understands pharma asset strategy and has demonstrated experience in area or global integrated evidence planning and subsequent planning of RWE studies/initiatives.
- Influencing/consultancy expertise: Strong influencing without authority skills. Demonstrated experience at coaching study teams or decision makers (expert and non-expert) through RWE study design decisions drawing upon scientific, strategic and practical needs.
- Working style: Individual must have demonstrated ability to work successfully in a cross-matrix setting. Skilled in consultant, team member and team lead working styles and able to flex working style to meet the specific project needs.
- Communication: Fluent at conveying complex information and context to expert and non-expert audiences in a clear and relevant manner. Compelling, adaptable communicator to small and large audiences across functions and levels of seniority.
- Project management: Ability to develop plans and self-manage timelines, resources, and deliverables effectively.
- Comfortable with the unknown: Must be comfortable to perform in previously uncharted territory with few, if any, established use cases, guidelines or processes. Flexibility to adjust based on changing circumstances and openness to new ideas and continuous learning.
- Therapeutic Area experience: oncology (heme, solid tumors), immunology or neurology indications strongly desired.
- Language: Must be fluent in English. Additional languages in relevant geographical region are desirable but not essential.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.
International RWE Lead employer: AbbVie
AbbVie is an excellent employer that values its employees by fostering a collaborative and inclusive work culture, particularly in the healthcare sector. With a strong emphasis on professional development, employees have access to numerous growth opportunities and training programs, making it an ideal place for those looking to advance their careers. Located in a vibrant area, AbbVie also offers unique benefits such as flexible working arrangements and a commitment to employee well-being.
StudySmarter Expert Advice🤫
We think this is how you could land International RWE Lead
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We think you need these skills to ace International RWE Lead
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at AbbVie!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show AbbVie that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at AbbVie!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At AbbVie, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at AbbVie
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at AbbVie that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with AbbVie’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
