Clinical Scientist

Job profile

Responsibilities will include:
• Initiate and support clinical studies with ScreenPoint products
• Develop and maintain relations with research partners
• Provide analysis support to effectively run clinical studies
• Collect report user feedback from study sites
• Bringing ideas for new use cases and value propositions
• Contribute to competitor analysis
• Support marketing activities
• Report on relevant scientific studies appearing in the literature
• Support QA/RA team with regulatory clearance process
• Present ScreenPoint’s achievement and research at congresses & exhibitions

Both technical and medical knowledge and experience in the field of (breast) medical imaging is vital. It is pivotal to gain deep understanding of Transpara, and the ability to communicate with different parties and stakeholders in clinical trials and studies. A hybrid way of working both at the office and from home is a possibility.

Minimum qualifications
• PhD Degree, with a medical background.
• Technical and clinical experience with medical imaging software applications.
• Organizational and networking skills
• Excellent verbal and written communication skills in Dutch and English
• Resourceful
• Strong interpersonal skills and the ability to build relationships internationally.
• Self-motivated with a high level of energy, enthusiasm and initiative.
• Readiness for (occasional) international travel.
• Flexibility regarding working times.

Preferred qualifications
• Experience with organizing clinical patient trials
• Analytical skills to analyze large data cohort
• Fluent in languages (other than English and Dutch) is a plus.

  • Accepted file types: pdf, doc, docx.
    Accepted file types are limited to .pdf and .doc only. Files sizes must be smaller than 5MB