The Medical Department provides value-added support to the organization in the areas of Clinical Research, Regulatory Affairs and Medical Services.

As a research-driven organization, we coordinate the conduct of worldwide multicentre clinical trials in local hospitals and institutions as part of Merck global drug development program. We are also responsible for the registration of our products with the Minisitry of Health Malaysia, allowing the Malaysian public access to new, breakthrough medicines. With patient safety as priority, we advocate strict compliance to the regulatory & corporate adverse experience monitoring and reporting requirements.

Within Medical Services, we ensure our promotional materials and activities meet and adhere to the highest ethical standards. Additionally, the Medical Department acts as the Medical & Scientific resource for the whole organization.

 The Medical Department is subdivided into 3 teams namely:

Clinical Research

Medical Services

Regulatory Services

MSD is a leading research-driven pharmaceutical company and thus recognizes the importance of clinical research which has helped to develop many of our Company’s breakthrough drugs.
 
Working in the Clinical Research Team, you are responsible for planning and executing clinical trials in designated trial centers throughout Malaysia. The data collected is important in helping the company define safety, tolerability and efficacy of our products which is necessary in helping to obtain the license to market new drugs in the country.
 
Success Factors

• Degree in Science/Pharmacy
• Previous pharmaceutical experiences - preferably in clinical research, would be advantageous
• Excellent communication and strong interpersonal skills

Fresh graduates are encouraged to apply.

Medical Services
Regulatory Affairs

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The Medical Services team provides timely, focused medical and scientific expertise to customers, both internal and external, through medical/product information and educational services.
 
You  are responsible in ensuring the accuracy of medical and product information that is channeled through either product leaflets or education seminars and provide analyses of the medical literature to support scientific basis for Merck informational and educational activities. You are also to ensure that our activities comply with legal and regulatory standards via medical legal review.

Clinical Research
Regulatory Affairs

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Before MSD is able to promote our breakthrough drugs to our customers, we need to comply with our local laws in registering the medicine with the Ministry of Health. The primary function of the Regulatory Affairs team is to achieve regulatory approval for medicines in the fastest possible time. This involves a complex integration of clinical research data and knowledge of regulatory processes in MSD and in the country.

As part of the Regulatory Affairs team, you are to ensure that the organization complies with the government regulations and make timely submission in the registration of our new and existing medications.

• Degree in Pharmacy and you must be a registered pharmacist
• Good problem solving and decision making skills
• Excellent communication skills