Job Summary

Associate Senior Clinical Data Insights Analyst

Are you passionate about supporting clinical trial technologies and ensuring smooth access to critical clinical data systemsDo you thrive in a collaborative, global environment where quality, compliance, and innovation are at the heart of everything you doIf so, you could be our next User Access Clinical Data Systems Associate at Novo Nordisk.

Your new role

As a Clinical Data Insight Analyst, you will play an important role in supporting the administration and maintenance of clinical data management systems across global clinical trials. You will be responsible for managing user access, configuring systems, supporting end-users, and ensuring compliance with applicable processes and regulatory requirements.

In this role, you will collaborate with stakeholders across Clinical Data Management, Clinical Operations, Biostatistics, Digital Innovation, and external vendors to deliver efficient and compliant solutions that support clinical trial execution.

Responsibilities

Managing site and user access across clinical data management systems such as EDC and eCOA platforms.
Creating, maintaining, and deactivating user accounts for internal and external stakeholders.
Performing configuration activities within user management tools and Veeva systems.
Managing rights, roles, study setup activities, and study closure/decommissioning processes.
Supporting incident management and resolving user access and system-related queries.
Ensuring documentation is maintained in accordance with company standards, SOPs, GCP, GDP, and GxP requirements.
Collaborating with cross-functional and global teams to meet project timelines and operational goals.
Contributing to process improvements and sharing best practices across teams and functions.

Your new department

In Research Development, you'll be part of a unit that explores bold scientific ideas and advances them into clinical testing. We combine curiosity, AI tools, and human data to develop transformative therapies. Through collaboration and operational excellence, we shape and deliver an innovative pipeline to meet future patient needs.

Within Clinical Data Management Programming (CDMP), you'll join a global team dedicated to delivering high-quality clinical trial data that enables evidence-based decision-making. Our culture of continuous learning and innovation drives us to implement new tools, systems, and processes that support the development of life-changing medicines for patients worldwide.

Qualifications

Bachelor's or Master's degree in Life Sciences, Computer Science, Information Technology, Clinical Information Management, or a related field.
2-3 years of experience within the pharmaceutical, biotechnology, clinical research, or healthcare industry.
Experience working with Clinical Data Management systems, user access management, vendor systems, or related platforms.
Knowledge of clinical trial processes and GxP requirements within drug development.
Strong understanding of computer systems, applications, and IT processes.
Excellent written and verbal communication skills in English.

Experience Level

Mid Level

Location

Bangalore

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.