Medical Content Specialist

Description

• Perform thorough medical review and approval of promotional and non ‑ promotional materials in Veeva Vault, ensuring alignment with:
• ZP-GSK medical and compliance standards
• Relevant Thai laws and regulations
• PReMA Code of Practice
• Provide clear, evidence ‑ based medical input and sign ‑ off on scientific and clinical claims, references, and risk ‑ benefit statements.
• Lead and deliver cross ‑ functional training on content approval processes, regulatory requirements, and ZP-GSK approval codes to commercial, marketing, and medical teams.
• Support development and maintenance of review checklists, templates, SOPs and guidance documents for content approval.
• Conduct management monitoring activities and maintain accurate records of review decisions.
• Track, escalate and follow up on corrective and preventive actions (CAPA) for material issues under the supervision of Medical Governance/CMD.
• Contribute to continuous improvement initiatives for the content approval process and systems (e.g., Veeva Vault configuration needs, workflow optimizations).

Qualifications

• Degree in a bioscience discipline or Pharmacy.
• Fluent English: able to read, write, speak and understand English. Able to interpret nuanced clinical and regulatory context in conversations and presentations.
• Strong medical knowledge of basic sciences and therapeutic areas including infectious disease, respiratory medicine and vaccine ‑ preventable illnesses.
• Excellent collaboration and communication skills; able to work effectively across multiple functions.
• Highly resilient with demonstrated learning agility and ability to manage competing priorities.