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 innovation.
- 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 51750 - 63250 £ per year.
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.
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.
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.
Global Medical Affairs Research Grant & Study Manager St Albans employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
StudySmarter Expert Advice🤫
We think this is how you could land Global Medical Affairs Research Grant & Study Manager St Albans
✨Get Involved with Local Health Initiatives
Join local community health events or volunteer for organisations like public health agencies. This not only builds your experience but also helps you network with industry professionals who might know of openings at places like Meeveem Limited.
✨Tap into Professional Associations
Check out associations like the Institute of Healthcare Management. They often have job boards, networking events, and conferences that are perfect for connecting with potential employers in health sciences administration.
✨Stay Updated with Industry Trends
Follow health policy news and trends—being knowledgeable about the current landscape will not only help you in interviews but also make you stand out as a candidate. You can discuss recent developments and their implications when chatting with folks at Meeveem Limited.
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We think you need these skills to ace Global Medical Affairs Research Grant & Study Manager St Albans
Some tips for your application 🫡
Highlight Your Relevant Experience:When applying for a role in health sciences administration, it's super important to spotlight any relevant experience you have in healthcare settings. Whether you've worked in a hospital, a clinic, or any related environment, make sure to detail those roles in your CV – focusing on your responsibilities and achievements that align with the job at Meeveem Limited.
Showcase Your Administrative Skills:Administrative skills are key in this field, so don’t hold back! Make sure your CV reflects your proficiency in things like scheduling, data management, and compliance with health regulations. Mention specific software you’ve used, such as patient management systems, as this will demonstrate your hands-on abilities and readiness for the role at Meeveem Limited.
Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to Meeveem Limited. Share a bit about why you’re drawn to this sector, any impactful situations or challenges you’ve encountered, and how they’ve shaped your desire to work in health sciences administration. This personal touch can really set you apart!
Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at Meeveem Limited. This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.
How to prepare for a job interview at Meeveem Limited
✨Showcase Your Administrative Skills
In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.
✨Know Your Regulations
Familiarity with healthcare regulations and compliance is crucial. Brush up on HIPAA, GDPR, or other relevant policies before your interview. We recommend preparing examples of how you've ensured compliance or handled sensitive information in past roles—this will show you're not just knowledgeable but also responsible.
✨Prepare for Scenario Questions
Interviews for administrative roles often involve scenario-based questions to assess your problem-solving skills. Practice responses to common situations you might face, such as dealing with a challenging patient or managing a sudden schedule change. This will not only demonstrate your ability to think on your feet but also highlight your interpersonal skills.
✨Align Your Goals with the Organisation
As a full-time candidate, employers will want to know how your long-term career goals align with their mission. Take some time to research Meeveem Limited’s values and be ready to tie your passion for health sciences administration into their objectives. Demonstrating enthusiasm and career alignment can be a game-changer in this competitive field!
