Clinical Research Associate

Welcome to Novo Nordisk, a world-renowned pharmaceutical company committed to improving the lives of patients living with chronic diseases. We are currently seeking a highly motivated Clinical Research Associate to join our team and play a critical role in developing life-changing treatments. As a Clinical Research Associate at Novo Nordisk, you will have the opportunity to collaborate with top researchers, physicians, and industry experts to bring innovative therapies to market. We are looking for individuals with a strong passion for clinical research, exceptional attention to detail, and a drive for continuous improvement. Join us in our mission to make a positive impact on the lives of millions around the globe.

1. Conduct clinical trials: The Clinical Research Associate will be responsible for planning, conducting, and monitoring clinical trials in accordance with standard operating procedures and regulations.
2. Collaborate with cross-functional teams: The candidate will work closely with cross-functional teams including researchers, physicians, regulatory affairs, and data management to ensure the successful execution of clinical trials.
3. Ensure compliance: The individual will ensure compliance with industry standards, company policies, and regulatory requirements throughout the clinical trial process.
4. Monitor study progress: The Clinical Research Associate will monitor study progress, identify and resolve any issues or delays, and provide regular updates to the project team.
5. Data collection and management: The candidate will be responsible for collecting, reviewing, and managing data from clinical trials, ensuring accuracy, completeness, and quality.
6. Maintain study documentation: The individual will be responsible for maintaining accurate and up-to-date study documentation, including protocols, study reports, and other study-related documents.
7. Identify and mitigate risks: The Clinical Research Associate will proactively identify potential risks and develop mitigation plans to ensure the successful completion of clinical trials.
8. Train and mentor team members: The candidate will provide training and guidance to team members on study protocols, data collection, and other study-related activities.
9. Continuous improvement: The individual will continuously evaluate and improve processes, procedures, and systems to increase efficiency and quality in clinical trial operations.
10. Represent Novo Nordisk: The Clinical Research Associate will represent Novo Nordisk in a professional manner at conferences, meetings, and other events related to clinical research.
11. Uphold ethical standards: The candidate will ensure that all clinical trials are conducted ethically and in accordance with applicable laws, regulations, and guidelines.
12. Travel: The individual may be required to travel to various clinical trial sites to monitor progress, conduct training, and ensure compliance with study protocols.

According to JobzMall, the average salary range for a Clinical Research Associate in 2880 Bagsværd, Denmark is approximately 40,000 to 60,000 DKK per month. This equates to roughly $6,000 to $9,000 USD per month. However, salaries may vary depending on the specific company, level of experience, and other factors. It is also important to note that the cost of living in Denmark is generally higher than in the US, so the equivalent salary in USD may not accurately reflect the standard of living.

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.