FAQs
What is the primary responsibility of a Clinical Research Associate (CRA) in this role?
The primary responsibility of a CRA is to oversee patient data and study-related information at clinical trial sites, ensuring compliance with research protocols, regulatory requirements, and good clinical practices.
Is this position home-based?
Yes, this position is home-based, allowing for flexibility in work location.
What are the travel requirements for this role?
There is a travel requirement of approximately 50% of the working time, which may include overnight stays within Germany.
What qualifications are required to apply for this position?
Candidates must have at least one year of experience as a Clinical Research Associate (CRA) and be fluent in both English and German, both spoken and written.
Will the CRA be involved in training activities?
Yes, the CRA is expected to participate in onboarding, indication, project-specific training, and general CRA training as needed.
What division does this role belong to?
This role belongs to the Development division of Novartis.
Can you explain the work environment of this position?
The work environment is a blend of home-based work and site visits to clinical research centers, promoting a dynamic and collaborative working atmosphere.
What company culture does Novartis promote?
Novartis promotes a culture of diversity, inclusion, and collaboration, striving to create a workplace that fosters innovation and allows employees to reach their full potential.
How does Novartis ensure compliance and risk management during the clinical trials?
The CRA manages compliance through continuous risk management, identifying center needs and issues early, and fostering a culture of adherence to GCP, protocols, and relevant regulations.
What support is available for applicants with disabilities?
Novartis provides the opportunity for applicants with disabilities to engage the local representative during the application process, and interested candidates should indicate this in their resume.