Job Description

Are you highly motivated by being able to make a difference in improving patients\xe2\x80\x99 lives? Are you a high-performing executive who is energized by challenges and able to influence people around you? If so, join the team and apply today!

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.

About the Department

The Clinical Medical Regulatory and Quality (CMRQ) department is one of the key functions that enable the business strategy through effective execution of functional goals, in the areas of Clinical Research, Medical Affairs, Regulatory, and Quality Assurance. The position of Clinical Research Associate is to be located in Kuala Lumpur, the capital of Malaysia, and report to the Clinical Team Lead / Clinical Operations Manager.

The Position

The role of the Clinical Research Associate is accountable for taking 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, ICH-GCP, company procedures, and protocol requirements to ensure data quality and study subject protection.
• You will be also be accountable for recruitment at the country/ site level and thereby delivers results that have a direct impact on the successful completion of the clinical program.
• You coordinate with the Project Manager and communicate to their progress and critical issues that may impair trial success.

Qualifications

• You hold a qualification in Degree in Medicine, Biology, Science, Pharmacy, Nursing, or another equivalent. You have a minimum of 2 years\xe2\x80\x99 solid operational experience in clinical development.
• Proactive communication both internally and externally is essential for the successful implementation of the main accountability. This position requires excellent social skills and good project management skills to achieve the success of acountable clinical trials.
• You are required to have a good comprehension of ICH-GCP, local requirements, and Novo Nordisk SOPs. You need to adapt and manage changes in the groups and/ or clinical trials that you are accountable for. You are required to travel within Malaysia. You are fluent in English (verbal and written) and Bahasa Malaysia.

Working at Novo Nordisk

At Novo Nordisk, we don\xe2\x80\x99t wait for change. We drive it. We\xe2\x80\x99re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development to manufacturing, marketing, and sales \xe2\x80\x93 we\xe2\x80\x99re all working to move the needle on patient care.

Contact

Please send your CV online (click Apply and follow the instructions).

Deadline

13 Jun 2023

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

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 for 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 communities we operate in. Together, we\xe2\x80\x99re life changing.

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