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Title:  Intern

Location: 

Petaling Jaya, MY, MY

Global Business Unit:  HEC
Job Function:  Regulatory Services
Requisition Number:  231700
Description: 

Job Summary

The Medical Intern will support the Medical Affairs function within our pharmaceutical organization, gaining meaningful hands-on exposure to the drug discovery, development, and commercialization process. Working under the guidance of experienced medical affairs professionals, the intern will contribute to real-world projects spanning medical information, clinical research support, regulatory compliance, and stakeholder engagement. This internship is designed to build scientific, clinical, and professional competencies that prepare candidates for a career in the pharmaceutical and life sciences industry.

General Responsibilities

1.     Medical Affairs Support

  • Assist in responding to medical information inquiries from healthcare professionals (HCPs), patients, and internal stakeholders in an accurate and evidence-based manner.
  • Help prepare and review medical communication materials, including scientific publications, slide decks, and educational content for HCPs and key opinion leaders (KOLs).
  • Support the Medical Science Liaison (MSL) team with background research, literature reviews, and preparation of scientific summaries for field engagements.

 

2.     Clinical & Scientific Research

  • Assist in monitoring and analyzing clinical data, laboratory results, and real-world evidence (RWE) relevant to the company’s therapeutic areas.

 

3.     Regulatory & Compliance

  • Assist in reviewing promotional and medical materials for regulatory compliance and scientific accuracy

 

4.     Stakeholder Engagement & Events

  • Assist in the planning and logistical coordination of medical advisory boards, scientific conferences, and regional/national trade events.
  • Provide administrative and scientific support during internal cross-functional project meetings and external stakeholder engagements.
  • Help develop and update materials for KOL engagement 

Functional Skills and Knowledge

  • Basic understanding of pharmaceutical product development, clinical trial processes, and regulatory frameworks.
  • Ability to search and critically appraise scientific and medical literature.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
  • Strong written and verbal communication skills; ability to convey complex scientific information clearly and concisely.
  • High attention to detail and commitment to accuracy in data handling and documentation

Education

  • Currently enrolled in or a recent graduate of an accredited programme in Medicine, Pharmacy, Pharmaceutical Sciences, Biochemistry, Life Sciences, or a related field.
  • Completion of at least one year of professional study with coursework relevant to clinical sciences, pharmacology, or drug development preferred.
Requisition Number:  231700
Job Function:  Regulatory Services

Apply now »