Are you a motivated professional with a passion for clinical research and a drive to make a difference in global healthcare? Novo Nordisk, a leading global healthcare company, is seeking a Senior Central Monitor to join their Centralised Monitoring Unit (CMU) in Bangalore, India. If you thrive in dynamic environments, enjoy collaborating with stakeholders, and have a can-do attitude, this could be the perfect opportunity for you. Apply now and become part of a team dedicated to improving patient lives worldwide.
About Novo Nordisk:
Novo Nordisk is a pioneer in healthcare with a 100-year legacy of combating chronic diseases like diabetes. With a presence in over 170 countries and impacting more than 40 million patient lives daily, Novo Nordisk is one of the most valuable companies globally. Their commitment to innovation, collaboration, and employee growth makes them a leader in the pharmaceutical industry.
Department Overview:
The Centralised Monitoring Unit (CMU) in Bangalore is a dynamic department within the Global Trial Portfolio area. It comprises skilled professionals, including medical reviewers, statistical monitors, functional programmers, and central monitors. The team focuses on Risk-Based Quality Management (RBQM), ensuring patient safety, data quality, and regulatory compliance. By leveraging advanced data visualization tools and analytical software, the CMU plays a critical role in proactive monitoring and risk mitigation across clinical trials.
Job Title: Senior Central Monitor
Location: Bangalore, India
Job Category: Clinical Development
Key Responsibilities:
As a Senior Central Monitor, you will play a pivotal role in ensuring the success of clinical trials by:
- Defining and monitoring Key Risk Indicators (KRIs) to ensure patient safety, data quality, and regulatory compliance.
- Performing ongoing centralized operational monitoring activities using vendor platforms and dashboards.
- Communicating findings to stakeholders and participating in project meetings to enable informed decision-making.
- Contributing to the implementation of RBQM strategies and driving continuous improvement initiatives.
- Mentoring and guiding junior monitoring staff to support their professional growth.
- Maintaining compliance with global and local SOPs, ICH/GCP guidelines, and regulatory requirements.
Qualifications:
To excel in this role, you should have:
- A bachelor’s degree in life sciences, healthcare, or a related discipline.
- 6+ years of clinical research experience with a strong understanding of the drug development process and RBQM principles.
- Prior experience as a CRA/Field Monitor and familiarity with analytical tools is desirable.
- Proficiency in aggregate data review and interpretation using visualization/analysis software.
- Strong communication, presentation, and cross-functional collaboration skills.
- A proactive mindset, attention to detail, and the ability to manage multiple priorities under tight deadlines.
Why Join Novo Nordisk?
At Novo Nordisk, you’ll be part of a culture that values collaboration, innovation, and employee growth. With over 63,000 employees worldwide, the company offers a supportive environment where your contributions make a real impact. By joining Novo Nordisk, you’ll be working toward a bigger purpose – improving the lives of millions of patients globally.
How to Apply:
If you meet the qualifications and are ready to take on this exciting challenge, apply now using Novo Nordisk’s online application tool. Don’t miss this opportunity to advance your career with a global leader in healthcare.
Application Deadline: 7th March 2025
