At a Glance
- Tasks: Lead global investigator-led research programs and manage clinical studies.
- Company: Join Mölnlycke, a leader in medical solutions with a mission to improve healthcare.
- Benefits: Permanent contract, competitive salary, flexible work, and a supportive culture.
- Other info: Diverse and inclusive workplace with opportunities for growth and innovation.
- Why this job: Make a real impact on healthcare outcomes and shape clinical evidence generation.
- Qualifications: 5+ years in clinical research; strong project management and stakeholder skills required.
The predicted salary is between 60000 - 75000 £ per year.
At Mölnlycke, we believe that real impact starts with people. People who are bold enough to challenge the status quo. People who care deeply for their work, their colleagues, and the world around them.
As a global medical solutions company, we design and deliver innovative products and services across wound care, operating room solutions, gloves, and antiseptics. Our mission is to advance performance in healthcare by supporting professionals, improving outcomes, and making a difference where it matters most.
Mölnlycke is seeking an Investigator-Led Research Program Manager to join our Clinical, Medical & Professional Affairs (CMPA) organisation, reporting to Global Clinical Compliance Director, and supporting the continued strengthening of our clinical compliance and governance approach globally. This is a highly visible, strategic role focused on leading and evolving our global investigator-led research program. You will oversee investigator-initiated studies (IIS), quality improvement projects (QIPs), and other site-led research activities that support evidence generation, clinical insight development, and innovation across our business.
Why This Role Matters
You will help define and elevate how investigator-led research is governed and delivered globally, strengthening our clinical compliance and governance approach while enabling high-quality evidence generation at scale.
Responsibilities
- Lead the end-to-end management of investigator-led research activities, including proposal review, governance, contracting, budget oversight, milestone tracking, and portfolio management.
- Partner with cross-functional stakeholders across CMPA, Regulatory, Commercial, and other relevant functions to ensure alignment with strategic evidence-generation priorities.
- Serve as the primary point of contact for external investigators and clinical sites, building strong scientific partnerships and ensuring compliant engagement.
- Drive operational excellence and continuous improvement across IIS, QIP, and other investigator-led research processes, tools, and governance frameworks.
- Monitor portfolio performance, proactively identify risks or delays, and implement corrective actions to ensure successful delivery.
- Support internal decision-making by providing portfolio insights, updates, metrics, and strategic recommendations.
- Contribute to the development of a long-term vision for investigator-led research within Mölnlycke.
- Act as Operational Process Owner (OPO) for investigator-led research processes and related site-led research support activities.
- Deliver training, guidance, and mentorship internally around IIS, QIP, and broader investigator-led research best practices.
- Identify and drive strategic enhancements across governance, workflows, and systems, contributing to the evolution of the Clinical Compliance function and strengthening efficiency, compliance, and overall program impact.
What You’ll Get
- Be part of a culture built on trust, care, and shared ownership—where you are empowered to make an impact, work with global experts, and contribute to the evolution of how clinical evidence generation and dissemination are governed and delivered.
- Your growth and development: You’ll gain experience that matters, in a company that’s clear on its mission and bold in its ambitions.
- Opportunity to shape and influence a global investigator-led research program.
- Exposure to senior cross-functional stakeholders and strategic initiatives.
- A collaborative international environment where innovation and continuous improvement are encouraged.
- The chance to make a measurable impact on clinical evidence generation and healthcare outcomes.
- Flexibility, wellbeing and benefits that reflect our commitment to you.
- Permanent contract.
- Competitive compensation and benefits package.
- International and collaborative work environment.
What You Bring
- We’re looking for a confident, experienced clinical research professional who thrives in a fast-paced, evolving environment and is motivated by building impactful programs and partnerships.
- Bachelor’s degree in life sciences, healthcare, or a related field; advanced degree (MSc, PhD, MD) preferred.
- Minimum 5 years of experience within clinical research, medical affairs, or related healthcare industry environments.
- At least 3 years of hands-on experience managing investigator-initiated studies (IIS) or comparable investigator-led research activities.
- Strong project or program management experience, including planning, budgeting, oversight, and cross-functional coordination.
- Experience within medical devices or other regulated healthcare environments.
- Working knowledge of EU MDR and ISO 14155 required, familiarity with IEC 62366 or global regulatory requirements, including FDA evidence expectations, preferred.
- Experience supporting or leading clinical investigations, clinical insight activities, clinical case studies, or quality improvement projects.
- Excellent stakeholder management and communication skills.
- Strong analytical and organisational capabilities.
- Ability to work effectively in a global matrix organisation.
- Fluent English, written and spoken.
Our approach to Diversity & Inclusion
We’re building a workplace where everyone feels seen, heard, and valued. We believe that a diverse mix of people — from different cultures, ages, geographies, and genders — makes us stronger. Inclusion isn’t just a value, it’s how we work, grow, and lead together.
About Mölnlycke
Mölnlycke is a world-leading medical products and solutions company that equips healthcare professionals to achieve the best patient, clinical and economic outcomes. Our business is organised in the four business areas Wound Care, Operating Room Solutions, Gloves and Antiseptics, where customer centricity, sustainability and digitalisation are at the heart of everything we do.
Mölnlycke employs around 8,700 people. The company headquarters are in Gothenburg, Sweden and we operate in more than 100 countries worldwide. Mölnlycke is a founding partner of GoCo Health Innovation City, a world-class innovation cluster for health.
Investigator-Led Research Program Manager in Oldham employer: Mölnlycke Health Care
At Mölnlycke, we foster a culture of trust and collaboration, empowering our employees to make a meaningful impact in the healthcare sector. As an Investigator-Led Research Program Manager, you will have the opportunity to shape global research initiatives while working alongside experts in a supportive environment that prioritises professional growth and innovation. With competitive benefits and a commitment to diversity and inclusion, Mölnlycke is an exceptional employer for those looking to advance their careers in a dynamic and impactful field.
StudySmarter Expert Advice🤫
We think this is how you could land Investigator-Led Research Program Manager in Oldham
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those connected to Mölnlycke. Attend industry events or webinars to make connections and learn more about their work culture.
✨Tip Number 2
Prepare for interviews by researching Mölnlycke's recent projects and initiatives. Show them you’re not just interested in the role but also in how you can contribute to their mission of advancing healthcare.
✨Tip Number 3
Practice your pitch! Be ready to discuss your experience with investigator-initiated studies and how you've driven operational excellence in past roles. Confidence is key!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining the Mölnlycke team.
We think you need these skills to ace Investigator-Led Research Program Manager in Oldham
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Investigator-Led Research Program Manager role. Highlight your relevant experience in clinical research and project management, and show us how you align with Mölnlycke's mission and values.
Showcase Your Achievements:When detailing your experience, focus on specific achievements that demonstrate your impact in previous roles. Use metrics where possible to quantify your success, as this will help us see the value you can bring to our team.
Be Clear and Concise:Keep your application clear and to the point. Avoid jargon and ensure your writing is easy to understand. We appreciate straightforward communication, so make it easy for us to see your qualifications and enthusiasm.
Apply Through Our Website:We encourage you to submit your application through our official website. This ensures that your application goes directly to us and allows you to easily track its progress. Plus, it’s the best way to stay updated on any further steps!
How to prepare for a job interview at Mölnlycke Health Care
✨Know Your Stuff
Make sure you’re well-versed in the specifics of investigator-led research and the regulatory frameworks like EU MDR and ISO 14155. Brush up on your knowledge about clinical compliance and governance, as this role is all about leading and evolving these processes.
✨Showcase Your Experience
Prepare to discuss your past experiences managing investigator-initiated studies or similar projects. Be ready to share specific examples of how you’ve driven operational excellence and continuous improvement in your previous roles.
✨Engage with Stakeholders
Since this role involves partnering with cross-functional teams, think about how you can demonstrate your strong stakeholder management skills. Prepare examples of how you’ve built scientific partnerships and ensured compliant engagement in your past work.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions that show your interest in the company’s mission and future direction. Inquire about their long-term vision for investigator-led research and how you can contribute to that journey.
