Biostatistician
Arbetsgivare / Ort:Mölnlycke Health Care AB / MÖLNDAL
Omfattning / Varaktighet:Tillsvidareanställning (inkl. eventuell provanställning) / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 4 oktober (13 dagar kvar)
Publicerad: 2026-09-04
Källa: Arbetsförmedlingen
Om jobbet
Biostatistician
Take your expertise further
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 now looking for a Biostatistician to our global HQ in Gothenburg.
Why This Role Matters
This is an opportunity to help generate the clinical evidence that supports innovative healthcare solutions and improves patient outcomes around the world.
As a Biostatistician within the Clinical Data and Statistical Science team, you will provide statistical expertise across the lifecycle of clinical studies, from study design through analysis and reporting. Working closely with clinical, medical, HEOR, data management and cross-functional teams, your insights will support evidence generation, scientific communication and key business decisions.
Here's how you'll make an impact
- Provide statistical input into clinical study designs, including sample size calculations and study methodology.
- Contribute to protocol development, Clinical Investigation Plans (CIPs) and Statistical Analysis Plans (SAPs).
- Develop, validate and quality control statistical analyses and outputs, preferably using R.
- Generate and review Tables, Listings and Figures (TLFs) for clinical studies.
- Support the preparation of Statistical Analysis Reports (SARs) and Clinical Investigation Reports (CIRs).
- Collaborate with Data Management teams to ensure data quality and analysis readiness.
- Interpret and communicate statistical findings to clinical, medical and business stakeholders.
- Ensure analyses are conducted according to applicable quality standards and Good Clinical Practice requirements.
What You'll Get
Be part of a culture built on trust, care and shared ownership
Join a global organization where collaboration, scientific excellence and patient impact are at the center of everything we do.
Your Growth and Development
You'll gain experience that matters, in a company that's clear on its mission and bold in its ambitions.
- Work on global clinical studies that contribute to better healthcare outcomes.
- Collaborate with experienced multidisciplinary teams across clinical research, medical affairs and data sciences.
- Develop your expertise in clinical evidence generation and medical device research.
- Contribute to publications, scientific communication and innovation initiatives.
Flexibility, Wellbeing and Benefits
- Flexible working arrangements in line with local policies.
- Competitive compensation and benefits package.
- Wellbeing initiatives and employee support programs.
- Opportunities for professional development and international collaboration.
What You Bring
Must Have
- MSc in Biostatistics, Statistics or a related field.
- Minimum 3 years of experience in statistics, preferably in medical devices, pharmaceutical, biotechnology or CRO environment.
- Solid understanding of clinical research methodology and study design.
- Strong statistical programming skills, preferably in R.
- Experience supporting clinical study analyses and statistical reporting.
- Strong communication skills and the ability to explain complex statistical concepts to diverse audiences.
- Fluent English, written and spoken.
- Ability to work effectively in cross-functional and global teams.
Nice to Have
- Experience with simulation methodologies or complex study designs.
- Contributions to scientific publications and regulatory submissions.
- Familiarity with medical device regulations.
- Experience supporting health economics or outcomes research activities.
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 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 worldwide. The company headquarters are in Gothenburg, Sweden, and it operates in more than 100 countries. Since 2007, Mölnlycke has been part of Investor AB, an engaged owner of high-quality global companies.
Arbetslivserfarenhet
- Biostatistiker (meriterande)
Arbetsgivare
Mölnlycke Health Care AB
Entreprenörsstråket 21
43153 MÖLNDAL
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Ansök senast 4 oktober (13 dagar kvar)