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- Tasks: Design and implement patient-centred outcomes strategies to enhance patient experiences.
- Company: Kyowa Kirin International, a forward-thinking pharmaceutical company focused on making a difference.
- Benefits: Inclusive culture, career development opportunities, and a chance to impact lives positively.
- Why this job: Join a team that pushes medical boundaries and prioritises patient care.
- Qualifications: Master’s degree in relevant fields and experience in patient-reported outcomes.
- Other info: Collaborative environment with opportunities to work with global regulatory agencies.
The predicted salary is between 36000 - 60000 ÂŁ per year.
At Kyowa Kirin International (KKI), our purpose is to make people smile. This means more than drug discovery and development; it is about embedding care into everything we do to make a difference every day for those that need it most. We’re an inclusive pharmaceutical company that takes time to understand what really matters to our patients, their families, and their healthcare professionals, helping our people to take bold actions that deliver life‑changing solutions sooner. Our culture is rooted in our values: Teamwork, Commitment to Life, Innovation, and Integrity.
Job Purpose
You will contribute to the design and delivery of patient‑centred outcomes (PCO) strategies and implementation across Kyowa Kirin’s global product portfolio. You will ensure that patient experience data, including Patient‑Reported Outcomes (PROs), is rigorously developed, implemented, analysed, and communicated to support regulatory, clinical, commercial, and real‑world evidence objectives. This role provides an opportunity to develop foundational expertise in PCO/PRO methods while working closely with senior PCO team members to advance patient centred measurement within Kyowa Kirin.
Key Responsibilities
- Contribute to PRO endpoint strategies across KK’s development programs, ensuring alignment with scientific, regulatory, and commercial needs.
- Provide PRO expertise for pipeline activities, as well as for real‑world evidence and prospective observational studies within KK’s portfolio.
- Manage qualitative and quantitative research activities, including concept elicitation, cognitive interviews, psychometric evaluation, and endpoint interpretation working with CROs.
- Partner with clinical operations, biostatistics, regulatory affairs, medical affairs, and commercial teams to ensure optimal design, implementation, and analysis of patient‑centric endpoints in clinical trials.
- Support strategic interactions with global regulatory agencies (FDA, EMA) by defining key PRO questions, preparing evidence packages, and ensuring responses reflect the latest scientific and regulatory expectations.
- Build and maintain strong relationships with academic researchers, key opinion leaders, industry consortia, and patient advocacy groups.
- Lead or contribute to high‑quality abstracts, posters, manuscripts, and conference presentations related to PRO/COA evidence.
- Build internal capability on patient‑centred measurement by coaching and educating cross‑functional colleagues on PCO best practices.
Position Requirements
- Master’s degree (or higher) in psychology, epidemiology, public health, outcomes research, or related discipline.
- Significant experience in PRO development, validation, and implementation in pharmaceutical and/or consulting environments.
- Preferably some experience interacting with FDA/EMA on patient‑focused measurement strategies.
- Demonstrated track record in designing and managing PRO studies across clinical trials and/or RWE settings.
- Deep understanding of FDA PFDD Guidances and global PRO regulatory frameworks.
- Knowledge of psychometric methods, PRO instrument development, scoring, and endpoint interpretation.
- Strong scientific writing skills for regulatory, scientific, and publication outputs.
Kyowa Kirin International is an equal opportunities employer. No agencies please.
Associate Director, Patient Centred Outcomes in Marlow employer: Kyowa Kirin International plc.
Contact Detail:
Kyowa Kirin International plc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Patient Centred Outcomes in Marlow
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at Kyowa Kirin. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for interviews by diving deep into patient-centred outcomes. Show us you know your stuff and can talk about how your experience aligns with our mission to make people smile.
✨Tip Number 3
Don’t just wait for job openings; be proactive! Keep an eye on our website and apply directly. We love seeing candidates who are genuinely interested in joining our team.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can leave a lasting impression and shows us you’re really keen on the role. Plus, it’s a great way to reiterate your passion for patient-centred outcomes.
We think you need these skills to ace Associate Director, Patient Centred Outcomes in Marlow
Some tips for your application 🫡
Show Your Passion for Patient-Centred Outcomes: When writing your application, let your enthusiasm for patient-centred outcomes shine through. We want to see how your values align with ours at Kyowa Kirin, so share your experiences that demonstrate your commitment to making a difference in patients' lives.
Tailor Your Application: Make sure to customise your CV and cover letter for the Associate Director role. Highlight your relevant experience in PRO development and any interactions you've had with regulatory bodies like the FDA or EMA. This will show us that you understand the specific needs of the position.
Be Clear and Concise: We appreciate clarity in applications! Use straightforward language and avoid jargon where possible. Make your points succinctly, especially when discussing your scientific writing skills and experience with PRO studies. This helps us quickly grasp your qualifications.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team at Kyowa Kirin!
How to prepare for a job interview at Kyowa Kirin International plc.
✨Know Your Patient-Centred Outcomes
Make sure you understand the key concepts of patient-centred outcomes and patient-reported outcomes. Brush up on the latest FDA and EMA guidelines, as well as any relevant psychometric methods. This will show that you're not just familiar with the terminology but can also apply it in real-world scenarios.
✨Showcase Your Collaborative Spirit
Since teamwork is a core value at Kyowa Kirin, be prepared to discuss your experience working with cross-functional teams. Share specific examples where you partnered with clinical operations, biostatistics, or regulatory affairs to achieve a common goal. Highlight how your collaborative efforts led to successful outcomes.
✨Prepare for Regulatory Discussions
Given the role's focus on strategic interactions with global regulatory agencies, think about your past experiences with FDA or EMA. Be ready to discuss how you've defined PRO questions or prepared evidence packages. This will demonstrate your understanding of the regulatory landscape and your ability to navigate it effectively.
✨Bring Your Scientific Writing A-Game
Strong scientific writing skills are crucial for this position. Prepare to discuss your experience in writing abstracts, posters, or manuscripts. If possible, bring samples of your work to showcase your ability to communicate complex information clearly and effectively, which is essential for regulatory and publication outputs.