FAQs
What is the primary responsibility of a Clinical Scientific Expert I at Novartis?
The primary responsibility of a Clinical Scientific Expert I is to provide clinical and scientific support throughout all phases of a clinical study, ensuring compliance with Novartis processes, ICH GCP, and regulatory requirements, while delivering study outcomes within schedule and budget.
What are the key performance indicators for this role?
Key performance indicators include the timely execution of assigned trials, effective operational planning with risk mitigation strategies, accurate clinical data review, high-quality contributions to study documents, and demonstrating Novartis values.
What qualifications are required for the Clinical Scientific Expert I position?
The minimum requirements include cross-cultural experience, operations management, project management, and skills in clinical research, trial protocol, data integrity, and risk monitoring.
Where is this position located?
This position is located in Hyderabad, India.
What kind of work experience is preferred for applicants?
Preferred work experience includes operations management and execution, collaboration across boundaries, and project management.
Is knowledge of multiple languages required for this role?
Proficiency in English is required; knowledge of other languages may be beneficial but is not specified as a requirement.
What does Novartis emphasize in its workplace culture?
Novartis emphasizes collaboration, support, and inspiration among employees to achieve breakthroughs that change patients’ lives, as well as building an inclusive and diverse work environment.
Are there any specific compliance standards that a Clinical Scientific Expert I must follow?
Yes, the role requires adherence to Novartis processes, ICH GCP, and other regulatory requirements in all clinical trial activities.
How does the Clinical Scientific Expert I contribute to the clinical trial team?
The Clinical Scientific Expert I is a core member of the Clinical Trial Team and may lead specific aspects of global clinical trials while assisting with program level activities and coordinating with relevant functions.
What kind of accommodations does Novartis provide for individuals with disabilities?
Novartis is committed to providing reasonable accommodations for individuals with disabilities during the recruitment process and employment. Individuals may contact Novartis for assistance if needed.