At a Glance
- Tasks: Lead evidence generation strategy and develop impactful research plans for healthcare stakeholders.
- Company: Join a leading pharmaceutical company focused on innovative healthcare solutions.
- Benefits: Competitive salary, comprehensive benefits, and opportunities for professional growth.
- Other info: Dynamic role with potential for career advancement and collaboration across global teams.
- Why this job: Make a real difference in healthcare by shaping evidence strategies that matter.
- Qualifications: Bachelor's degree in relevant field and extensive experience in healthcare research.
The predicted salary is between 80000 - 116600 £ per year.
About the Role
In this Associate Director level role, you will help shape and deliver the evidence generation strategy for the United Kingdom and Ireland. You will play a key role in identifying local evidence gaps and translating them into scientifically rigorous, feasible, patient-focused, and compliant plans that address the needs of healthcare stakeholders and decision-makers. As part of the Global Evidence Generation organization, you will connect local priorities with regional and global evidence planning, research priorities, and investment decisions. Your work will contribute to high-quality real-world evidence, observational research, database studies, research collaborations, and investigator-initiated research. You will also help strengthen evidence planning and execution through innovative thinking, digital technologies, advanced analytics, and artificial intelligence-enabled approaches.
How You Will Contribute
- Lead evidence generation strategy by identifying and prioritizing local evidence gaps with medical, market access, and cross-functional partners.
- Guide research across the study lifecycle from concept development and governance review through execution, analysis, reporting, close-out, and dissemination.
- Develop scientific study materials with internal experts and external partners, including protocols, analysis plans, reports, abstracts, and manuscripts.
- Ensure scientific quality and compliance by applying company policies, ethical standards, research practices, and relevant regulatory requirements.
- Coordinate integrated evidence planning with local, regional, and global partners across medical, research, access, regulatory, data, and operational functions.
- Manage the evidence portfolio by overseeing priorities, budgets, forecasts, contracts, vendors, timelines, performance, and material risks.
- Build strategic scientific relationships with healthcare professionals, patient organizations, institutions, investigators, networks, and scientific societies.
- Apply digital and analytical capabilities to strengthen evidence planning, portfolio oversight, communication, and execution.
Qualifications
- Bachelor's degree in medicine, pharmacy, life sciences, public health, epidemiology, health economics, or a related field.
- Ten to twelve years of relevant experience in the pharmaceutical industry, healthcare research, academia, or a related environment.
- Demonstrated leadership of evidence generation activities, including non-interventional, real-world evidence, observational, database, or other Medical Affairs studies.
- Strong knowledge of evidence generation strategy, research methods, good research practices, and applicable ethical and regulatory requirements.
- Strong understanding of United Kingdom healthcare systems, health technology assessment requirements, reimbursement decisions, and evidence needs.
- Ability to translate medical and healthcare questions into clear evidence needs and executable research plans.
- Strong scientific judgment and experience evaluating study designs, data, analyses, and scientific outputs.
- Professional fluency in English with strong project, portfolio, vendor, budget, stakeholder influence, matrix leadership, communication, and digital skills.
Location
While a primary location is identified for this role, qualified internal candidates in other locations may also be considered, subject to business needs, role requirements, and local employment considerations.
Compensation
The salary range displayed reflects the primary location associated with this posting. Compensation may vary for candidates considered in other locations. Where applicable, location-specific salary ranges and compensation information will be provided in accordance with local requirements.
Locations
London, Great Britain
Base Salary Range £84,800.00 - £116,600.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Worker Type Employee
Worker Sub-Type Regular
Time Type Full time
Evidence Generation Lead, Uk & Ireland employer: Takeda
At Takeda, we pride ourselves on being an exceptional employer that fosters a culture of collaboration and innovation. As a Global Medical Excellence Lead based in the UK, you will benefit from a supportive work environment that prioritises employee growth through continuous learning opportunities and impactful projects. Join us to make a meaningful difference in healthcare while enjoying a dynamic workplace that values your contributions and encourages professional development.
StudySmarter Expert Advice🤫
We think this is how you could land Evidence Generation Lead, Uk & Ireland
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We think you need these skills to ace Evidence Generation Lead, Uk & Ireland
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 Takeda!
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 Takeda 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 Takeda!
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 Takeda, 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 Takeda
✨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 Takeda that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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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 Takeda’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.
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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.