Clinical Research Associate

"Are you a motivated and detail-oriented individual with a passion for making a difference in the healthcare industry? Novo Nordisk is seeking a Clinical Research Associate to join our dynamic team. As a global leader in diabetes care and other chronic diseases, our mission is to improve the lives of millions of people worldwide. In this role, you will play a crucial role in the development and execution of clinical trials to ensure the safety and efficacy of our products. If you are driven, organized, and have a strong understanding of clinical research processes, we invite you to apply for this exciting opportunity."

1. Conduct and oversee clinical trials: The Clinical Research Associate will be responsible for managing and coordinating clinical trials to ensure they are conducted in compliance with protocols, regulations, and company standards.
2. Monitor trial progress: The individual will monitor the progress of clinical trials and identify any issues or challenges that may impact the trial timelines or results.
3. Ensure compliance: The CRA will ensure that all trial activities are conducted in compliance with relevant regulations, guidelines, and standard operating procedures.
4. Data collection and analysis: The individual will be responsible for collecting, analyzing, and reporting data from clinical trials to assess safety and efficacy of products.
5. Manage trial documentation: The CRA will maintain and manage trial documentation, including informed consent forms, case report forms, and other essential documents.
6. Build relationships: The individual will collaborate with cross-functional teams and build relationships with investigators, site staff, and other stakeholders to facilitate smooth trial execution.
7. Perform site visits: The CRA will conduct site visits to ensure that trial procedures are being followed accurately and to resolve any issues that may arise.
8. Train site staff: The individual will provide training and support to site staff on trial procedures, study protocols, and other relevant topics.
9. Ensure patient safety: The CRA will be responsible for monitoring the safety of trial participants and reporting any adverse events to the appropriate authorities.
10. Participate in study meetings: The individual will participate in study team meetings to provide updates on trial progress and discuss any issues or challenges.
11. Stay updated on regulations: The CRA will stay updated on relevant regulations and guidelines to ensure that all trial activities are conducted in compliance with current standards.
12. Contribute to process improvement: The individual will identify areas for process improvement and contribute to the development and implementation of new processes and procedures.
13. Adhere to ethical standards: The CRA will adhere to ethical standards and maintain confidentiality of all trial-related information.
14. Represent the company: The individual will represent the company at conferences

According to JobzMall, the average salary range for a Clinical Research Associate in Copenhagen, Denmark is between 35,000 DKK to 55,000 DKK per month. This translates to approximately $5,500 to $8,600 USD per month. However, this can vary depending on factors such as level of experience, specific industry, and company size.

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.