Novartis, a global healthcare leader, offers an exciting opportunity for professionals to contribute to transformative clinical research as a Clinical Scientific Expert I. This role blends scientific excellence with operational expertise, driving innovation in clinical trials to deliver life-saving therapies. Here’s a closer look at this career-defining position:
About Novartis
Novartis is a pioneer in reimagining medicine, leveraging cutting-edge science and technology to address complex health challenges. With a robust global presence, Novartis is dedicated to improving patient outcomes through innovation, integrity, and collaboration. The company fosters an inclusive culture where diverse perspectives thrive, driving its mission to extend and improve lives worldwide.
Responsibilities in the Job
As a Clinical Scientific Expert I, you will play a pivotal role in advancing clinical trials. Your key responsibilities include:
- Study Management: Contribute to global clinical trial activities, ensuring adherence to schedules, budgets, and quality standards.
- Data Analysis and Insights: Perform clinical data review to identify trends, signals, and risks related to trial endpoints and patient safety.
- Documentation: Assist in creating study documents, including protocols, informed consent forms (ICF), and clinical sections of Clinical Trial Applications (CTA).
- Cross-functional Collaboration: Coordinate with data management, drug supply management, clinical development teams, and Country Pharma Organizations.
- Issue Resolution: Develop and implement resolution plans for identified issues.
- Compliance: Ensure adherence to Novartis processes, ICH-GCP guidelines, and regulatory requirements.
- Risk Management: Proactively plan operational contingencies and risk mitigation strategies.
Qualifications
To excel in this role, candidates must meet the following qualifications:
- Educational Background: A degree in life sciences or related fields.
- Experience:
- Cross-cultural collaboration.
- Operational management and execution.
- Project management.
- Industry Expertise: Knowledge of clinical trial protocols, data integrity principles, and regulatory frameworks.
Key Skills
Successful candidates should possess:
- Expertise in clinical research and clinical trials management.
- Proficiency in risk monitoring and trends analysis.
- Strong abilities in data review and insights generation.
- Exceptional communication skills, with fluency in English.
