Select Page

Requirements for the position of Flying Study Nurse

Requirements for the position of Flying Study Nurse at Camovis GmbH:

Essential Requirements (Critical Success Factors):

  • Customer-oriented mindset
  • Willingness to travel
  • Driver’s license and readiness for flights
  • Readiness for deployment, flexibility, adaptability, and resilience
  • High self-motivation in home office work
  • Structured and independent work approach
  • Ability for optimal time management
  • Strong organizational and planning skills
  • Friendly and competent demeanor, along with effective communication skills
  • Basic knowledge of English, both spoken and written

Desirable Requirements:


  • Completed training as a medical assistant (Arzthelfer/in) or MFA (Medical Assistant) or nurse/paramedic
  • Ideally, additional training as a Study Nurse or comparable experience in the field of clinical research
  • ICH-GCP certificate or at least basic knowledge
  • Proficiency in Microsoft Office (Outlook, Office, Word)
  • Friendly and well-groomed appearance
  • Excellent German language skills
  • Keen eye for details and a high standard of accuracy
  • Reliability
  • Strong sense of responsibility

Skills you will acquire during the orientation period:

  • Fluent English language skills
  • Laboratory tasks (collecting vital signs, conducting EKGs, blood withdrawals, s.c. and i.m. injections)
  • Study Nurse certificate
  • IATA certificate

Tasks and Responsibilities:


  • Supporting and coordinating interdisciplinary clinical studies at various research centers throughout Germany
  • Communication with sponsors, CROs, and sites
  • Close collaboration and reporting with sites and the team
  • Flexible deployment for limited timeframes
  • Coordination of study visit activities (time planning, ensuring necessary materials, creating source documents following the study protocol)
  • Assistance during patient visits, including extensive diagnostics and laboratory assistance
  • Collection of laboratory samples and conducting tests on study participants (blood withdrawals, EKG readings, spirometry, vital parameters)
  • Documentation of medical data in CRFs and internet-based databases
  • Thorough, GCP-compliant, and precise documentation
  • Creation, maintenance, and expansion of databases and matrices
  • Appointment and document organization
  • Participation in reporting adverse events
  • Participation in and preparation for initiation and monitoring visits
  • Preparation, assistance, and follow-up during inspections and audits

Core Values:

  • Trust
  • Transparency
  • Openness
  • Innovation
  • Team spirit