Clinical Research Associate

The position The role of the Clinical Research Associate is taking the leadership of site management for the selection and initiation of sites. Other role tasks are as follows, but are not limited to: Conduction and closing activities of the appointed studies in compliance with local regulations, International Conference on Harmonization-Good Clinical Practice (ICH-GCP), company procedures, and protocol requirements to ensure data quality and study subject protection. You will manage the recruitment at the country/ site level and thereby deliver results that have a direct impact on the successful completion of the clinical program. You partner with the Project Manager and report on their progress and critical issues that may impair trial success. Qualifications Degree in Medicine, Biology, Science, Pharmacy, Nursing, or another equivalent. You have a minimum of 2 years' solid operational experience in clinical development. Excellent interpersonal skills and good project management skills to achieve the success of assigned clinical trials. A good understanding of ICH-GCP, local requirements, and Novo Nordisk Standard Operating Procedures (SOPs). Proactive communication both internally and externally is essential for the successful implementation of the main accountability. Able to adapt and manage changes in the groups and/ or clinical trials that you are assigned with. You are required to travel within Malaysia and fluent in English (verbal and written) and Bahasa Malaysia. Working at Novo Nordisk At Novo Nordisk, we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company in the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds, and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and the communities we operate in.