- 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.
- 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.
Clinical Research Associate - Kuala Lumpur, Malaysia - Novo Nordisk A/S
Description
Are you highly motivated by being able to make a difference in improving patients' lives? Are you a high-performing executive who is energized by challenges and able to influence people around you? In Novo Nordisk Malaysia, the position of Clinical Research Associate provides you the opportunity to work in a high-performing team to contribute directly towards the business results while creating values for Diabetes patients. Join us and apply today for a life-changing career
Joining a Talent Pipeline in Novo Nordisk
You are applying to be part of the Novo Nordisk Talent Pool. We are currently not interviewing for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in the future, please submit your CV.
Joining our pipeline means that you will be considered a potential match for all current and upcoming Clinical Research Associate roles. By applying, we'll match your profile on a continuous basis against all suitable positions to ensure you don't miss out on a life-changing career. When an opportunity arises, we will reach out and invite you for an interview. We will keep your application for six months ensuring the best opportunities to provide a solid match for open positions.
If you want to be considered for the Clinical Research Associate position, we look forward to receiving your application.
About the department
The Clinical, Medical, and Regulatory (CMR) department is one of the key functions that enable the business strategy through the effective execution of functional goals, in the areas of Clinical Research, Medical Affairs and Regulatory. The position of Clinical Research Associate is to be located in Kuala Lumpur, the capital of Malaysia, and will report to the Clinical Team Lead.
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:
Qualifications