Are you a person with innovative thinking and proactive attitude with continuous improvement as one of your career objectives? Join GSC Global Development Team at Novo Nordisk and get a life-changing career!
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.
Job Title : Clinical Data Manager / Biostatistics and Data Management
Requisition ID : 38249BR
About the department
GD-GSC-Data Management Unit supports Projects and Trial Management on operational Data Management activities of clinical projects. The key objective of the department is to ensure high quality data delivery to the stakeholders. The involvement of various groups in data management is significant in key stages of trial setup, conduct and closeout. The major activities handled include CRF Design, Database set-up & Programming, Data Entry, Data Validation, Medical Coding, Lab data handling, Data analysis & migration, Database Lock, Hyperlinking and Bookmarking and Project Management. These opportunities have in turn fostered a deeper understanding with an ability to drive, contribute to process and share
best practices while leveraging cross-cultural collaboration towards a unified mission to achieve clean data.- To Ensure integrity of clinical trial database.
- Perform Data Validation ensuring completeness and clean data.
- Ensure availability of data to relevant stakeholders.
- Write, send, update, and resolve data clarifications.
- Create test cases and test validation procedures.
- Perform UAT of the database.
- Generate reports and communicate with stake holders in a timely manner
- Understand and comply with all applicable standard operating procedures and working instructions.
- Develop and maintain good communications and working relationships with Data Management team.
- Assist in timely scanning, book marking and indexing of documents in novoDOCS
- Ensure good documentation practices are followed.
Qualifications
- Masters or Bachelor degree in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science or clinical information management or equivalent qualifications.
- The candidate should have around 3 years of data management experience and the majority of this within Pharmaceutical Industry or Development.
- Preferably knowledge of Clinical Development and Project Management.
Note : Freshers and candidate without Clinical Data Management experience need not apply.
