SENIOR CLINICAL AFFAIRS & RESEARCH SPECIALIST, DENMARK

Responsibilities

Danish Country Clinical Affairs:

• Actively building and maintaining optimal relationships with danish customers and customer representatives, as well as Key Opinion Leaders and danish local authorities, medical & scientific communities and the medical device industry focusing on the assigned therapeutic areas
• Representing Medtronic as “the Clinical face” in Denmark and acting at the same time as the “voice” of the danish customers and authorities towards stakeholders at Medtronic for the assigned therapeutic areas
• Mapping internal, external and environmental barriers and developing plans to address them in a methodical way

Support in Study Management, Study Execution and External Research Program (ERP):

• Oversee the clinical Project Portfolio for Denmark and deliver high-quality to meet stakeholders’ needs and expectations
• Coordinating with investigators the ERP submission, tracking, and local administration all in alignment with existing Standard Operating Procedures (SOP’s) 

Local Danish evidence dissemination & awareness:

• Ensuring awareness of Danish clinical activity and new clinical evidence and providing input to Medtronic sales & marketing leaders
• Advising Danish covering marketing organization on outcome of publications and provide suggestions on relevant communication strategy
• Providing clinical evidence on ongoing tenders  

Must Haves

• Bachelor’s or Master’s degree in relevant technical, clinical or biomedical field
• Fluent in Danish and English.
• Wide and in-depth knowledge of Danish evidence needs and Danish law & regulations within Clinical Affairs
• General knowledge of ‘Good Clinical Practice’ and applicable regulations
• 5+ of relevant experience in the Clinical Affairs and/or Clinical Research
• Ability to see the bigger picture and have global perspective on Clinical Affairs
• Good judgmental sense, decisive, commercial attitude, outstanding problem solving & influencing competences
• Enjoys to work in a cross-functional team and within a matrix organization
• Experienced project manager and scientific writer
• Committed & comfortable to ensure strict adherence to regulations