Life Sciences Central Monitor Job at Novo Nordisk
Location: Bangalore, India
Job Category: Clinical Development
Department: Centralised Monitoring Unit (CMU)- Bangalore
If you thrive in a dynamic environment and enjoy challenges, then we have a great opportunity for you. Novo Nordisk is seeking a Life Sciences Central Monitor to join our growing team. In this role, you will work in an international environment with key stakeholders to ensure patient safety and data quality in clinical trials. If you have a can-do attitude and a passion for continuous improvement, apply now!
About the Department
The Centralised Monitoring Unit (CMU)- Bangalore is a department within the Clinical Drug Development area of Novo Nordisk. It consists of skilled medical professionals and technical programmers who collaborate to ensure overall patient safety and wellbeing in clinical trials. The department focuses on risk-based medical monitoring, operational data visualization, and detection of unusual data patterns, errors, compliance issues, or fraud across trials.
In this role, as a Central Monitor, you will have the following responsibilities:
- Define standard and trial-specific key risk indicators (KRI’s) and perform ongoing monitoring of operational risks.
- Ensure appropriate definition of KRI’s impacting patient safety, data quality, and regulatory compliance.
- Perform ongoing centralised operational monitoring activities using vendor platform dashboards/outputs.
- Communicate findings of operational reviews to relevant stakeholders and participate in project meetings.
- Contribute to discussions and share learnings with colleagues and other stakeholders.
- Maintain compliance with global and local SOPs, GCP, and other regulatory requirements.
- Bachelor’s degree in life sciences, scientific, or healthcare discipline.
- Minimum 3 years of relevant clinical research experience with knowledge of drug development process and risk-based quality management principles.
- Prior CRA/Field Monitoring and analytical tool experience is desirable.
- Skills in aggregate data review and interpretation using visualization/analysis software.
- Strong understanding of clinical trial design, execution, and operations.
- Excellent communication and presentation skills.
- Ability to manage multiple projects and priorities effectively.
- Strong analytical skills with a quality mindset.
- Ability to work collaboratively in cross-functional and diverse teams.
- Proactive, detail-oriented, and resilient to changes.
Contact: To submit your application, please upload your CV and motivational letter online.
Deadline: 15th December 2023
Novo Nordisk is committed to an inclusive recruitment process and equality of opportunity for all job applicants.
Keywords: Life Sciences Central Monitor, Novo Nordisk, Bangalore, Clinical Development, Centralised Monitoring Unit, Medical Reviewers, Functional Programmers, Statistical Monitors, Operational Monitoring, Risk-Based Medical Monitoring, Data Visualization, Clinical Trial Design, GCP, Regulatory Compliance. Life Sciences Central Monitor Job at Novo Nordisk. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebook