Clinical Research Associate

Novo Nordisk

Clinical Research Associate executing Novo Nordisk trials in Malaysia for diabetes, obesity, cardiometabolic, and rare disorders. Monitoring sites, recruitment, safety, data integrity, and regulatory compliance.

Posted 8/13/2026full-timeKuala Lumpur • 🇲🇾 MalaysiaJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in conducting and managing clinical studies in compliance with ICH-GCP and local regulations, with a strong focus on patient safety and data integrity. Proficient in project management and effective communication, ensuring successful collaboration with research sites and multifunctional teams.

Highest-signal resume keywords

Clinical Research Associate ExperienceICH-GCP KnowledgeProject Management SkillsFluency in EnglishFluency in Bahasa Malaysia

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ManagementData MonitoringAdverse Event HandlingData Discrepancy ResolutionRegulatory Compliance

Soft Skills

Interpersonal SkillsProactive CommunicationAdaptability

Industry Keywords

Clinical DevelopmentDiabetes ResearchObesity ResearchCardiometabolic DisordersRare Disorders

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conduct and close assigned clinical studies in compliance with local regulations, ICH-GCP, company procedures, and protocol requirements
Manage recruitment at the country/site level
Monitor site data to ensure patient safety and data integrity
Resolve data discrepancies
Handle adverse events in accordance with regulatory requirements
Partner with the Project Manager and report progress and critical issues that may impair trial success
Manage site relationships from site selection through study closure
Collaborate with research sites and global multifunctional teams
Contribute to clinical studies advancing treatments for diabetes, obesity, cardiometabolic, and rare disorders

Requirements

What you’ll need

Degree in Medicine, Biology, Science, Pharmacy, Nursing, or another equivalent field
Minimum of 2 years’ solid operational experience in clinical development as a Clinical Research Associate
Excellent interpersonal skills
Good project management skills
Good knowledge of ICH-GCP, local requirements, and Novo Nordisk SOPs
Proactive internal and external communication skills
Ability to adapt and manage changes across multiple clinical trials
Required to travel within Malaysia and potentially Singapore and Thailand
Fluency in English, both verbal and written
Fluency in Bahasa Malaysia

Benefits

Comp & perks

Mentorship from experienced CRAs
Continuous learning opportunities
Professional growth and development
Inclusive recruitment process and equality of opportunity