Clinical Evidence Specialist
Mölnlycke Health Care AB / Biomedicinjobb / Göteborg
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If you're ready to have an impact in a career that makes a difference, Mölnlycke could be your next step. You'll be helping to equip medical professionals around the world with solutions to improve outcomes for patients. And you'll be developing yourself in a global environment with an inspirational culture, with lots of opportunities. All the while building a successful career, with real purpose.
Mölnlycke is looking for a Clinical Evidence Specialist to play a crucial role in executing Clinical Evaluations, PMCF planning and providing clinical perspective input to cross-functional teams in new product development and life cycle management for Mölnlycke 's medical devices.
In this job you will be based at our headquarters in Gothenburg and very soon at our new office at GoCo Health Innovation City, a world-class innovation cluster for health!
About the job
This is a great opportunity to contribute to our product development process and life management activities with regards to clinical evidence and PMCF input (Clinical Evaluation Plans, Clinical Evaluation Reports and PMCF documentation).
These are the main accountabilities for this position
Grow your career in an international environment! In this position you'll provide clinical evidence knowledge and input for Mölnlycke 's medical devices.
You'll work cross-functionally and provide relevant clinical input to project development projects and life cycle management activities.
You'll be the SME for clinical evidence input to the technical documentation for assigned products.
You'll search, review and appraise clinical literature and information specifically applicable to clinical performance and safety of Mölnlycke 's medical devices.
You'll provide input to Post Market Follow-up strategies for Mölnlycke 's medical devices .
You'll evaluate clinical evidence to support clinical performance and safety including support for Claims and Marketing messages.
You'll provide support and be the SME for Clinical Evaluations and PMCF during internal and external audits.
What you'll need
In this role we would like you to have the following capabilities, qualifications and experience:
PhD (in relevant medical/scientific area) OR Relevant medical/scientific degree + 5 years ' relevant experience in the medical device industry OR + 10 years ' relevant experience in the medical device industry.
Experience from Medical Device or Pharmaceutical Industry preferably within Clinical Research/Clinical Evaluations.
Analytical thinking and scientific mindset, knowledge in MDR, relevant MDCG guidance documents and MEDDEV standards for Clinical Evaluations and PMCF.
Experience in systematic literature search strategies, critical appraisal of clinical studies,, proficient scientific writing and with a digitalization mindset.
To be successful in this role you'll need to have the ability to act in a transparent and consistent manner while driving results, be a problem solver and solution-oriented with evidence of risk-adjusted decision making and to have good networking and organizational skills as well as sense of ownership and execution. You'll need to be a strong team player who can manage multiple and diverse stakeholders and to have strong and clear communication skills utilized to reach decisions that balance a diverse set of needs.
You'll need to be fluent in English (both written and spoken).
What you'll get
Wellness benefits
Flexible working hours
Great colleagues in a global company
An open, friendly and fair working atmosphere
Competitive compensation package including company pension plan, bonus, company health care
Our approach to diversity and inclusion
At Mölnlycke diversity is not just a vision, but our strength. We are dedicated to fostering an inclusive workplace that values and celebrates the power of diversity. At the heart of our commitment is the belief that diversity fuels innovation, creativity and problem-solving. We invite you to be a part of a team where authenticity is embraced, and every employee, regardless of background or any other traits, experiences a true sense of belonging. Your attitude, drive, enthusiasm, and eagerness to learn are just as important to us as the requirements for the role.
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 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, and in early 2025 our headquarters will move there. 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/careersIf this sounds like you and you feel you have what it takes to succeed in this role, we want to hear from you as soon as possible.
Så ansöker du Sista dag att ansöka är 2024-11-01
Klicka på denna länk för att göra din ansökan Omfattning Detta är ett heltidsjobb.
Arbetsgivare Mölnlycke Health Care AB (org.nr 556547-5489)
Gamlestadsvägen 3 C (
visa karta)
402 52 GÖTEBORG
Arbetsplats Mölnlycke Health Care AB
Jobbnummer 8933354
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