Lead change that lasts
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.
People who know exactly why they do what they do.
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 won’t just manage projects. 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.
In this role, you will:
-
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
This role is ideal for someone who brings strong clinical research expertise, strategic thinking, and stakeholder leadership, along with a passion for shaping and scaling impactful, well-governed research programs in a complex global environment.
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. It brings fresh perspectives, drives better decisions, and helps us deliver solutions that reflect the world we serve. 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. Since 2007, the company has been part of Investor AB, an engaged owner of high-quality, global companies which was founded by the Wallenberg family in 1916. For more information, please visit Mölnlycke and Mölnlycke Careers
