Clinical Evidence Manager in Oldham

Drive impact at scale

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.

• Why This Role Matters
• Mölnlycke is now looking for a

Clinical Evidence Manager (Wound Care) to join our Clinical Medical & Professional Affairs (CMPA) team.

In this highly visible global role, you will shape and lead clinical evidence strategies that support innovation, strengthen market access, and drive commercial success across our Wound Care portfolio.

You’ll join a global team with a shared mission: to advance performance in healthcare.

• Here’s how your contributions will shape meaningful outcomes
• Lead the development and execution of Evidence Planning for assigned Wound Care portfolios, ensuring evidence strategies remain aligned throughout the product lifecycle.
• Act as the key clinical evidence partner to Wound Care R&D, Marketing, Commercial and Regulatory stakeholders, translating business needs into robust evidence generation plans.
• Serve as the CMPA representative within product development projects, supporting evidence needs from concept through lifecycle management.
• Lead cross‑functional evidence strategy teams, driving collaboration, alignment and successful execution of clinical evidence activities.
• Provide expert clinical and scientific guidance within the wound care field and serve as a trusted point of contact for dedicated areas.
• Identify evidence requirements to support new product development, regulatory submissions, market access and competitive differentiation.
• Partner with Clinical Operations and Clinical Data & Statistical Sciences teams on clinical study design and evidence generation activities.
• Monitor, interpret and leverage scientific literature, medical intelligence and clinical data to support informed decision‑making and strategy development.
• Provide recommendations on Investigator Initiated Studies and ensure alignment with overall evidence strategies.
• What You’ll Get
• A strategic global role with the opportunity to directly influence clinical evidence generation for innovative wound care solutions.
• Exposure to senior stakeholders across R&D, Marketing, Commercial, Regulatory and Medical Affairs functions.
• Opportunities to shape the future direction of clinical evidence and market access strategies within a global healthcare leader.
• A collaborative and international environment where expertise, innovation and continuous learning are valued.
• Flexibility, Wellbeing and Benefits That Reflect Our Commitment to You
• Permanent role.
• Flexible and hybrid working arrangements where applicable.
• Competitive compensation and benefits package.
• Wellbeing initiatives that support your physical, mental and financial wellbeing.
• Career development opportunities within a global organization committed to internal growth and mobility.

What You Bring

• Must‑Haves
• Relevant medical, scientific, life sciences or healthcare‑related education, preferably at Master's degree level.
• Extensive experience within Medical Affairs, Clinical Affairs, Clinical Research or Scientific Affairs in the medical device industry.
• Strong understanding of clinical evidence generation, evidence strategy development and product lifecycle management.
• Demonstrated ability to lead complex cross‑functional initiatives and influence diverse stakeholder groups.
• Strong analytical thinking and scientific mindset, with the ability to translate data into actionable recommendations.
• Excellent communication, presentation and stakeholder management skills.
• Strong organizational skills, a proactive approach and an entrepreneurial sense of ownership.
• Commercial awareness combined with a passion for improving patient outcomes through evidence‑based healthcare solutions.
• Fluent written and spoken English.
• Nice‑to‑Haves
• Experience within wound care or adjacent therapeutic areas would be a plus.
• Experience supporting market access strategies is an advantage but not required.
• Familiarity with global regulatory and reimbursement evidence requirements would be beneficial.
• Experience working within global matrix organizations is an advantage.
• 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 Go Co 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 www. molnlycke. com and www. molnlycke. com/careers .

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