Novartis Job Vacancy For Clinical Research Associate
Position Purpose:
• Experienced specialists performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of assigned clinical trials.
• Is responsible to deliver data within timelines and required quality standard, responsible for adherence to monitoring procedures in accordance with GCP and ICH, local regulations and SOPs.
Major Accountabilities:
• Monitors patient data and study-related information related to clinical study sites and clinical trial participation.
• Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan.
• Provides timely and accurate monitoring of patient data and study-related information from source documents, research records, and site visits where applicable.
• May monitor study sites and audit facility selection.
• Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial
• Performs site Initiation Visit, ensures site personnel is fully trained on all trial related aspects
• Applies company policies and procedures to resolve a variety of issues
• Frequent internal company and external contacts.
• Represents organization on specific projects
• Contributes to some cost center goals and objectives
• Is the frontline liaison between Novartis and sites to ensure successful collaboration, site engagement and meeting Novartis expectation on milestone and deliveries
• Deliver customer satisfaction results for internal and external customers
• Delivery of Clinical Trials to quality standards and agreed timelines
• Adherence to Novartis policy and guidelines and external regulations
How this role will Impact our purpose:
This role will be responsible for overseeing & monitoring trial related activities at the site, thereby ensuring robust site management and overall quality & data integrity at the clinical trial sites.
Minimum requirements :
• Operations Management and Execution Project Management Cross Cultural Experience
• Bachelor’s degree in any specialization. (Desirable) – Bachelor’s in Pharma/ Life Science.
• Minimum 1 to 2 years of relevant experience as CRA.
• Fluent in both written and Spoken English.
Why consider Novartis?
799 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.
Imagine what you could do at Novartis!
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