Clinical Research Associate

Welcome to Novo Nordisk, a global healthcare company dedicated to improving the lives of millions living with chronic diseases. We are currently seeking a highly motivated Clinical Research Associate to join our team and help drive forward our groundbreaking research projects. As a Clinical Research Associate, you will play a crucial role in ensuring the success and safety of our clinical trials, making a direct impact on the lives of patients worldwide. We are looking for individuals with a strong scientific background, exceptional attention to detail, and a passion for making a difference in the field of healthcare. If you are ready to take on a challenging and rewarding role at a leading company in the industry, we encourage you to apply for this opportunity.

1. Conduct thorough and accurate review and monitoring of clinical trial data, including patient records, laboratory results, and adverse events, in accordance with company and regulatory guidelines.
2. Collaborate with cross-functional teams to plan, execute, and track clinical trial activities, including site selection, enrollment, and data collection.
3. Ensure compliance with all applicable laws, regulations, and protocols to maintain the integrity and ethical standards of the clinical trials.
4. Identify and communicate potential risks or issues to the appropriate stakeholders, and implement corrective actions as needed.
5. Review and maintain trial documents and essential study site files, ensuring completeness, accuracy, and timeliness.
6. Act as the primary point of contact for study sites, providing training, support, and guidance to site personnel as needed.
7. Coordinate and facilitate study site initiation, monitoring, and close-out visits, ensuring timely completion of all required activities.
8. Maintain a high level of knowledge and understanding of the study protocol, therapeutic area, and disease states to effectively support study activities.
9. Participate in the development and review of study-related documents, such as protocols, informed consent forms, and study reports.
10. Support the preparation and conduct of internal and external audits and inspections, providing necessary support and data as requested.
11. Keep accurate and up-to-date records of all study-related activities, including site communications, monitoring visits, and data collection.
12. Adhere to company standard operating procedures and best practices to ensure consistent and high-quality work.
13. Contribute to the continuous improvement of processes and procedures to increase efficiency and effectiveness in clinical trial execution.
14. Maintain confidentiality of all patient and company information in accordance with company policies and regulatory requirements.
15. Act as a representative of the company and uphold its values and reputation in all interactions with internal and external stakeholders.

According to JobzMall, the average salary range for a Clinical Research Associate in Philadelphia, PA, USA is between $60,000 and $85,000 per year. This can vary depending on factors such as years of experience, education level, and specific industry or company.

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.