At a Glance
- Tasks: Lead global research grant programs and manage investigator-initiated studies.
- Company: Join Santen, a global leader in eye health with over 130 years of expertise.
- Benefits: Competitive salary, flexible working, and a commitment to diversity and inclusion.
- Other info: Empower your career in a dynamic, inclusive environment focused on eye health.
- Why this job: Make a real impact on patient outcomes through innovative research initiatives.
- Qualifications: 5+ years in Medical Affairs or Clinical Research with strong governance experience.
The predicted salary is between 63000 - 77000 £ per year.
Company Description: Santen is a specialized company with a proud 130-year heritage focused exclusively on eye health. As a Japan-originated, global company with our footprint in over 60 countries and regions, our mission is to provide essential and significant value to patients and society through our products and services created from our expertise in ophthalmology and from the patient's perspective.
Job Description: We are seeking an experienced Global Medical Affairs Research Grant & Study Manager to join our Global Medical Affairs team. This is a unique opportunity for a Medical Affairs or Clinical Research professional with deep expertise in Investigator-Sponsored Studies (ISS/IST) and research grants to play a pivotal role in shaping Santen's global evidence-generation strategy. The successful candidate will take direct ownership of investigator-initiated research programs and serve as a key partner to Medical Affairs, Clinical Development, Compliance, Legal and external research stakeholders. The role focuses on generating high-quality evidence through investigator-led studies, Phase IV research, registries, observational studies, and real-world evidence initiatives while ensuring robust governance, compliance, and operational excellence.
What you will do:
- Lead Global ISS and Research Grant Programs
- Own and manage the end-to-end lifecycle of Investigator-Sponsored Studies (ISS/IST) and research grant programs.
- Coordinate proposal intake, scientific review, governance processes, contracting, milestone tracking, reporting requirements, and payments.
- Ensure studies are executed in compliance with company policies, ethical standards, and applicable regulations.
- Maintain inspection-ready documentation and provide oversight throughout study execution.
- Drive Medical Affairs Evidence Generation
- Lead operational support for Medical Affairs-sponsored evidence generation activities across multiple regions.
- Manage Phase IV studies, observational research, registries, post-authorization studies, and real-world evidence (RWE) initiatives.
- Monitor timelines, budgets, deliverables, risks, and study performance to ensure successful execution.
- Support dissemination of study outcomes through publications, presentations, and scientific communications.
- Bridge Clinical Development and Medical Affairs
- Partner closely with Clinical Development and Clinical Operations teams to support Phase III programs and facilitate seamless transition into post-approval research.
- Contribute to evidence-generation planning, investigator engagement, and study feasibility activities.
- Ensure alignment between development-stage research and Medical Affairs evidence-generation objectives.
- Build Strong External Partnerships
- Act as a trusted partner to investigators, academic institutions, healthcare professionals, research organizations, and key opinion leaders.
- Support collaborative research initiatives that advance scientific knowledge and improve patient outcomes.
- Work with CROs and external vendors to ensure quality delivery and operational excellence.
Qualifications:
- 5+ years of experience in Medical Affairs, Clinical Research, Clinical Operations, Evidence Generation, or a related field.
- Strong experience managing Investigator-Sponsored Studies (ISS/IST) and research grant programs.
- Proven expertise in research grant governance, including review processes, contracting, milestone management, reporting, and payment oversight.
- Demonstrated experience in Medical Affairs evidence generation, including Phase IV studies, registries, observational research, and real-world evidence programs.
- Experience collaborating with Clinical Development teams and supporting the transition from Phase III clinical programs to post-approval research.
- Experience working with investigators, academic institutions, KOLs, CROs, and external research partners.
Education & Qualifications:
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, Public Health, or another relevant scientific discipline.
- Advanced scientific degree (PhD, PharmD, MPH, MSc) preferred.
- Strong working knowledge of GCP, ICH guidelines, and clinical research regulations.
- Fluent English communication skills.
What we offer:
Competitive Salary: A market‐aligned base salary starting from 78.863 GBP – 108.436 GBP, depending on experience and location.
Ready to make a difference? Apply today and help us shape the future of eye health.
Additional Information:
Grow your career at Santen. A career at Santen is an opportunity to make a difference. We aspire to contribute to the realization of "Happiness with Vision" by providing eye health products and services to patients, consumers, and medical professionals around the world. Guided by our CORE PRINCIPLE, "Tenki ni sanyo suru", Santen is engaged in the global research & development, manufacturing, and sales and marketing of pharmaceutical products in ophthalmology. We have team members around the world using their diverse talents to unlock new modalities and drive innovations for patient outcomes, education and treatment. At Santen, we believe in empowering all our team members with flexible ways of working and a highly inclusive work environment.
The Santen Group is an Equal Opportunity Employer. We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs, role requirements and individual qualifications regardless of race, color, ethnicity, national origin/ancestry, religion, sexual orientation, gender, gender identity/ expression, age, disability, medical condition, marital status, veteran status, or any other characteristic protected by law.
If you require any kind of accommodation during our recruitment process, please let the recruiter from our team know.
Summary Type: Full-time Function: Research Experience level: Mid-Senior Level Industry: Pharmaceuticals
Global Medical Affairs Research Grant & Study Manager in St Albans employer: Santen Incorporated
Santen is an exceptional employer dedicated to advancing eye health, offering a collaborative and inclusive work culture that empowers employees to make a meaningful impact. With a strong focus on professional growth, Santen provides ample opportunities for career development and innovation in a global setting, ensuring that team members can thrive while contributing to the well-being of patients worldwide. Located in a vibrant environment, employees benefit from competitive salaries and flexible working arrangements, making Santen a truly rewarding place to work.
StudySmarter Expert Advice🤫
We think this is how you could land Global Medical Affairs Research Grant & Study Manager in St Albans
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We think you need these skills to ace Global Medical Affairs Research Grant & Study Manager in St Albans
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 Santen Incorporated!
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How to prepare for a job interview at Santen Incorporated
✨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 Santen Incorporated 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.
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