Clinical Evidence Manager – Wound Care
- Candidates should reside in Eastern or Central Time zone
Some roles generate evidence. This role decides what evidence matters.
Mölnlycke is 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.
As a strategic partner across the organization, you'll help transform innovative product concepts into evidence-backed solutions that can succeed in global markets. Working closely with colleagues in R&D, Regulatory Affairs, Medical Affairs, Health Economics, and Marketing, you'll determine what clinical, pre-clinical, and health economic evidence is needed, guide projects through key decision points, and influence outcomes long before a product reaches healthcare professionals and patients.
Success in this role requires more than scientific expertise. It calls for sound judgment, strategic thinking, and the ability to balance regulatory requirements, commercial objectives, patient needs, risk, cost, and timing.
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:
Compensation & Benefits:
This role offers a competitive base salary and annual bonus! Offers of employment consider various factors including experience, education, location, and role-specific requirements.
Our comprehensive benefits package is designed to support your health, financial well-being, and work-life harmony:
- Medical, dental, and vision plans are available from your first day of employment and provide extensive coverage through multiple options so you can find the right fit for you and your family.
- Financial benefits include a robust 401(k) plan with company match, profit sharing, tuition reimbursement, life insurance and both flexible spending accounts and health savings accounts.
- Molnlycke offers generous paid time off, paid parental leave, an Employee Assistance Program and lifestyle perks like discounted access to entertainment and travel
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 organized in the four business areas Wound Care, Operating Room Solutions, Gloves and Antiseptics, where customer centricity, sustainability and digitalization 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 www.molnlycke.com and www.molnlycke.com/careers.