Clinical Research Coordinator

Are you passionate about making a difference in the field of healthcare and shaping the future of medical treatments? Do you have a strong background in clinical research and a desire to work for a global pharmaceutical company with a commitment to improving the lives of patients? If so, we have an exciting opportunity for you to join our team at Novo Nordisk as a Clinical Research Coordinator. As a key member of our research team, you will play a critical role in facilitating and coordinating clinical trials to advance the development of innovative therapies. We are seeking a highly motivated and organized individual with excellent communication skills and a keen attention to detail. If this sounds like you, we encourage you to apply for this rewarding position and be a part of our mission to make a positive impact on the world of healthcare.

1. Facilitate and coordinate clinical trials to advance the development of innovative therapies.
2. Collaborate with internal teams and external partners to ensure smooth and efficient execution of clinical research studies.
3. Maintain accurate and up-to-date records of study progress and data.
4. Ensure compliance with all applicable regulations and guidelines.
5. Communicate effectively with study participants, healthcare professionals, and other stakeholders.
6. Assist in the recruitment and screening of potential study participants.
7. Develop and maintain relationships with key opinion leaders in the medical community.
8. Conduct literature reviews and stay abreast of developments in the field of healthcare.
9. Analyze and interpret clinical data to support decision-making.
10. Continuously monitor and report on study progress, including any issues or concerns that may arise.
11. Contribute to the development and implementation of study protocols and standard operating procedures.
12. Train and mentor junior research staff as needed.
13. Adhere to ethical and safety standards in all aspects of study conduct.
14. Represent the company at conferences and other industry events.
15. Maintain confidentiality of all study-related information.
16. Take an active role in the improvement of study processes and procedures.
17. Contribute to the writing and review of study reports and publications.
18. Act as a liaison between study sites and the company.
19. Ensure timely completion of all study-related tasks and deliverables.
20. Embrace the company's mission and values and demonstrate a commitment to making a positive impact on the world of healthcare.

According to JobzMall, the average salary range for a Clinical Research Coordinator in Clayton, NC, USA is between $47,000 and $63,000 per year. This may vary depending on factors such as experience, education, and specific job responsibilities.

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.