Job Description

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Clinical Medical Manager

Category: Clinical Development and Medical

Location:

Kuala Lumpur, Kuala Lumpur, MY

Are you looking for an opportunity to utilize your medical knowledge to communicate scientific data and interact with medical global thought leaders? Are you passionate about the world of clinical trials? Are you highly motivated by being able to make a difference in improving patients' lives? If so, you should continue reading and apply today!

About the Department

The Clinical Medical Regulatory and Quality (CMRQ) 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, Regulatory, and Quality Assurance.

A significant part of the person's job at the start will be to proactively assess the feasibility of conducting the New Therapy Areas (NTA) trials under the given assumptions and engage with Key Opinion Leaders (KOL) and investigators at the peer level, which will have a strong impact of the company and the patient's future.

You will be reporting to the CMRQ Director.

The Position

As Clinical Medical Manager, you will facilitate the execution of clinical trials related to New Therapy Areas (including Cardiovascular Disease (CVD), Non-alcoholic Steatohepatitis (NASH), Chronic Kidney Disease (CKD), Mild Cognitive Impairment (MCI) and Alzheimer's disease) by providing medical/scientific expertise and advice based on interactions with KOL, independent professional associations, and patient advocacy associations as necessary. You will cover the whole of Malaysia, Thailand, and Singapore.

Your main responsibilities will be:

• To identify and map KOLs, investigators, and research centers within the relevant therapy areas and collaborate closely with clinical operations teams during the feasibility and allocation process.
• To collect and discuss relevant early development data with external medical and scientific experts optimizing the feasibility process for the clinical trial conduct and providing leadership in the scientific community within New Therapy Areas by conducting advisory boards, scientific meetings, and engaging with local associations for HCPs on relevant topics.
• To contribute to delivering successful clinical trials (phase I-IV) in collaboration with clinical operations including driving scientific discussions at site selection and initiation visits, performing ad hoc visits, supporting investigator meetings, ensuring KOL inclusion in clinical trials, and engaging key investigators to communicate trial results.
• To provide timely medical guidance and internal training by supporting content creation and delivering training to clinical staff.
• To engage in scientific communication. The position requires extensive scientific communication internally as well as externally and excellent and proactive communications skills are a necessity.

Qualifications

In order to be considered for this role, you need to have an MD or Ph.D. in healthcare with a strong clinical and preferably research background. A pharmacy degree can also be considered.

Other requirements are:

• A solid 5 - 6 years or more of clinical, research, and pharmaceutical industry experience.

• Good understanding of drug development processes and relevant background in clinical research: e.g. as CRA, clinical trial investigator, or sub-investigator. Alternatively, you may have covered clinical trials in a Medical Affairs role.
• Expert in the therapeutic area of relevance, preferably with authorship in peer-reviewed journals.
• Understanding of the specificities and nuances of the local healthcare infrastructure.

Working at Novo Nordisk

At Novo Nordisk, we don't wait for change. We drive it. We're 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 - we're all working to move the needle on patient care.

Contact

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

Deadline

11 November 2022

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 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. Together, we're life-changing.