At a Glance
- Tasks: Lead medical strategy and drive innovation in patient care.
- Company: Rosemont Pharmaceuticals, a trusted name in liquid medicines for over 50 years.
- Benefits: Annual bonus, healthcare cash plan, flexible working, and generous leave.
- Other info: Join a diverse team committed to inclusion and personal growth.
- Why this job: Make a real impact on global healthcare and improve patient outcomes.
- Qualifications: Medical degree required; experience in Medical Affairs or Clinical Development preferred.
The predicted salary is between 94500 - 115500 £ per year.
- Medical Director
- We Are Rosemont
For over 50 years, Rosemont Pharmaceuticals has been a trusted name in the development and manufacture of oral liquid medicines.
With a portfolio of over 130 products - including 70 licensed medicines - we’re proud to support healthcare professionals and patients, especially those with swallowing difficulties.
Our purpose is clear: to improve patient outcomes through innovation in liquid formulations.
We’re highly respected across the pharmaceutical industry and have played a key role in establishing best practices for dysphagia care.
Our mission is to create a globally connected, people-focused organisation where every individual is empowered to thrive and achieve their best.
If you're passionate about making a meaningful impact to patients across the world and want to be part of a company with a strong heritage and ambitious vision, we’d love to hear from you.
About the Role
We are seeking an experienced and visionary Medical Director to join our Scientific Affairs function and support shaping the future of our medical and clinical strategy.
This is a high-impact leadership position responsible for driving medical affairs excellence, providing scientific inputs across our product portfolio, and ensuring patient safety remains at the heart of everything we do.
As a key scientific leader within Rosemont, you will act as the primary medical interface with healthcare professionals, key opinion leaders, patient communities, and external stakeholders.
You will play a pivotal role in influencing future product development by translating unmet medical needs, clinical insights, and patient perspectives into strategic opportunities.
This is a hybrid position and would require the successful candidate to work from our Leeds facility 2-3 days a week.
Key Responsibilities
- Medical Affairs & Scientific Leadership
- Develop and lead the global medical affairs strategy aligned to business and R&D objectives.
- Provide medical leadership across pipeline and marketed products.
- Support target product profiles, clinical development plans, and lifecycle management activities.
- Ensure all medical affairs activities remain compliant, ethical, and evidence-based.
- Healthcare Professional & KOL Engagement
- Build and maintain strong relationships with key opinion leaders, investigators, and clinical experts.
- Lead scientific exchange activities, including advisory boards, investigator meetings, and congress engagement.
- Gather and translate clinical insights into development and commercial strategies.
- Support publication planning and scientific communication activities.
- Medical Review & Compliance
- Act as the final medical signatory for promotional and non-promotional materials.
- Ensure all communications comply with ABPI Code of Practice, MHRA requirements, and all applicable regulations.
- Provide medical review and approval of claims, references, and scientific content to ensure communications are compliant, non-misleading, and aligned with the product licence and approved prescribing information.
- Partner with Commercial, Marketing, Regulatory Affairs, and Compliance teams to deliver accurate, balanced, and compliant scientific communications.
- Patient Advocacy & Engagement
- Develop meaningful partnerships with patient organisations and advocacy groups.
- Ensure patient perspectives are integrated into development strategies and benefit-risk assessments.
- Support patient-focused programmes, educational initiatives, and disease awareness activities.
- Pharmacovigilance & Patient Safety
- Provide executive leadership for pharmacovigilance and safety governance activities.
- Oversee compliance with global pharmacovigilance regulations and requirements.
- Review safety data, risk management plans, and benefit-risk evaluations.
- Ensure safety insights inform product development, labelling, and risk minimisation activities.
- Leadership & Governance
- Participate in key governance committees and development review boards.
- Collaborate across Clinical Development, Regulatory Affairs, Quality, and Commercial functions.
- Support due diligence, licensing opportunities, and strategic partnerships.
- Mentor and develop medical affairs and pharmacovigilance teams to foster scientific excellence and compliance.
About You
To succeed in this role, you will be a highly credible medical leader with a passion for scientific innovation, patient outcomes, and strategic healthcare engagement.
Essential Qualifications & Experience
- Medical Degree (MD) required.
- Specialist medical training or Ph D highly desirable.
- Significant experience within Medical Affairs, Clinical Development, or related pharmaceutical functions.
- Proven success leading medical strategy for pipeline and/or marketed products.
- Strong experience with pharmacovigilance and safety governance frameworks.
- Demonstrated capability engaging healthcare professionals and key opinion leaders at a regional or global level.
- Experience incorporating patient insights into product development and lifecycle management activities.
- Key Competencies
- Strategic mindset with the ability to influence business and unmet patient need
- Strong leadership and decision-making capabilities.
- Excellent stakeholder management and relationship-building skills.
- Outstanding scientific communication and presentation skills.
- High ethical standards and commitment to patient safety and compliance.
Benefits
At Rosemont, we believe great benefits go beyond salary. That’s why our offering is shaped by what our people truly value:
- Annual Bonus
- Recognising your contribution to Rosemont.
- Healthcare Cash Plan
- Personal cover to support your health and wellbeing
- 3% Employee / 5% Company Pension Contribution
- Helping you plan for the future
- 26 Days Annual Leave + Bank Holidays
- Flexible Working
- Including hybrid and flexible working hours available.
- Free On-Site Parking
- Convenient access to our Leeds facility
- Rosemont Rewards Platform
- Discounts, free perks, and wellbeing tools for all employees
We are committed to fostering an environment of enablement where our people can grow, develop their talents, and pursue meaningful career paths.
By placing patients and customers at the heart of everything we do, we drive high performance through accountability, consistency, and a strong governance structure.
We champion inclusion, community, and a rewarding employee experience - creating a culture that supports development, celebrates achievement, and empowers individuals to thrive.
Diversity & Inclusion is integral to our culture and reflecting the patients we serve.
At Rosemont, we believe equal opportunity for all is fundamental to our company's values and all our applicants can expect fairness and transparency in our recruitment process.
Ready to Make a Difference?
If you are an experienced medical leader looking to shape healthcare innovation, influence future product development, and improve outcomes for patients worldwide, we'd love to hear from you.
Apply today and join Rosemont in delivering life-changing medicines to patients who need them most!
Medical Director in Bradford employer: Rosemont Pharmaceuticals
Rosemont Pharmaceuticals is an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. With a focus on employee growth, we provide opportunities for professional development while working alongside senior leadership in a fast-paced environment. Our hybrid working model in Leeds ensures a healthy work-life balance, making it an ideal place for those seeking meaningful and rewarding careers in finance.
StudySmarter Expert Advice🤫
We think this is how you could land Medical Director in Bradford
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We think you need these skills to ace Medical Director in Bradford
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 Rosemont Pharmaceuticals!
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 Rosemont Pharmaceuticals that you're not just a fit for the job but also a safety-conscious candidate!
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How to prepare for a job interview at Rosemont Pharmaceuticals
✨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 Rosemont Pharmaceuticals 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 Rosemont Pharmaceuticals’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.
