Join our team at Novo Nordisk as a Clinical Data Manager and make a meaningful impact on the lives of patients worldwide. In this role, you will utilize your expertise in data management to ensure the accuracy, completeness, and integrity of clinical trial data, supporting the development of life-changing treatments. We are looking for a detail-oriented and collaborative individual with a strong background in data management and a passion for improving patient outcomes. If you are driven by a mission-driven purpose and thrive in a fast-paced and dynamic environment, we want to hear from you.
- Ensure accuracy, completeness, and integrity of clinical trial data through meticulous data management processes.
- Collaborate with cross-functional teams to develop and maintain data management plans and protocols.
- Monitor and review data to identify and resolve discrepancies or errors.
- Develop and implement data cleaning and validation processes to ensure high-quality data.
- Participate in data review meetings and provide updates on data status and potential issues.
- Maintain and update data management systems and databases.
- Ensure compliance with regulatory requirements and industry standards for data management.
- Support the development of new data management processes and procedures to improve efficiency and accuracy.
- Train and mentor junior data management staff and provide guidance on best practices.
- Communicate effectively with internal and external stakeholders to address data-related issues and concerns.
- Contribute to the development of study protocols and case report forms to ensure data collection meets study objectives.
- Proactively identify and implement solutions to improve data quality and streamline data management processes.
- Develop and maintain data management documentation, including data validation plans, data transfer agreements, and data management plans.
- Keep up-to-date with industry trends and developments in data management and apply best practices to improve processes.
- Prioritize and manage multiple projects simultaneously, ensuring timely and accurate delivery of data management activities.
Bachelor's Or Master's Degree In A Related Field Such As Biostatistics, Clinical Research, Or Data Management.
At Least 3 Years Of Experience In Clinical Data Management, Preferably In The Pharmaceutical Or Biotech Industry.
Strong Understanding Of Fda Regulations And Ich/Gcp Guidelines Related To Clinical Data Management.
Proficiency In Data Management Software And Tools Such As Oracle Clinical, Sas, And Medidata Rave.
Excellent Communication And Project Management Skills, With The Ability To Work Effectively In A Team Environment And Manage Multiple Projects Simultaneously.
Project Management
Data Analysis
Database Management
Quality Control
Data cleaning
Risk assessment
Regulatory compliance
Clinical Trials
Protocol Development
Electronic Data Capture
Clinical Data Management System (Cd
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Teamwork
Active Listening
Adaptability
Problem-Solving
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Novo Nordisk AS engages in the research, development, manufacture, and marketing of pharmaceutical products. It operates through the Diabetes and Obesity Care; and Biopharmaceuticals segments. The Diabetes and Obesity Care segment covers insulins, glucagon-like-peptide 1, other protein-related products, oral anti-diabetic drugs and obesity. The Biopharmaceuticals segment handles the research, development, manufacture, and distribution of products within the areas of haemophilia, growth hormone, hormone replacement, inflammation and other therapy areas.

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