Life Sciences Job | Novo Nordisk Hiring | Apply Online
Explore a rewarding opportunity in Life Sciences Jobs with Novo Nordisk as an Associate Clinical Data Facilitator. This role is crucial in managing clinical data, ensuring seamless operations in clinical trials, and contributing to the advancement of healthcare. Ideal for those seeking to enhance their Novo Nordisk Career, this position offers a chance to work at the forefront of Clinical Data Management (CDM) and drive impactful change in the pharmaceutical industry.
- Job Title – Associate Clinical Data Facilitator
- Department – Data Standards and Integration
- Location – Bangalore
About the Company
Novo Nordisk is a global healthcare company with over 100 years of innovation and leadership in diabetes care. This organization is committed to driving change to defeat diabetes and other serious chronic conditions such as obesity, and rare blood and endocrine disorders. Headquartered in Denmark, Novo Nordisk employs more than 45,000 people in 80 countries and markets its products in around 170 countries. The company focuses on scientific excellence to develop solutions that meet the needs of patients worldwide.
Key Responsibilities
- Performing site user access management across data management systems such as EDC and eCOA, including creating, maintaining, and removing user accounts for external and internal stakeholders
- Configuring and maintaining settings in user management tools, including uploading rights and roles, importing reports, and managing deployment files
- Providing day-to-day business support and incident management, delivering technical expertise to resolve operational issues
- Coordinating with global teams and cross-functional stakeholders to ensure effective process management and standardisation across trials
- Maintaining study versions in end-user systems and performing study closure, lock, and decommission activities
- Promoting the exchange of knowledge within the department through share-better-practice sessions and trial-related meetings
Qualifications
- A Master’s or Bachelor’s degree in Life Science, or equivalent qualifications
- Minimum 2–3 years of experience in the pharmaceutical industry, preferably within Clinical Data Management systems, vendor management, or related areas
Skills Required
- Knowledge of GxP guidelines and regulatory requirements within drug development, including SOPs, GCP, and GDP
- Strong planning, coordination, and analytical skills with a quality-first mindset and the ability to work independently
- Fluency in written and spoken English, with cultural sensitivity and the ability to collaborate effectively in a diverse, global environment
- Experience with project management, stakeholder communication, and presentations is an advantage
Deadline: 5th August 2025.
A Career in Life Sciences Jobs at Novo Nordisk offers the opportunity to be at the forefront of innovation in healthcare. As an Associate Clinical Data Facilitator, you play a pivotal role in Clinical Data Management (CDM), ensuring the integrity and accuracy of trial data. This position not only enhances your Novo Nordisk Career but also contributes significantly to advancing healthcare solutions worldwide. Join Novo Nordisk to be part of a legacy that impacts generations.
