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