• Act as scientific expert in the key therapeutic categories for external stakeholders.
• Build and maintain scientific trust-based relationships with KOLs.
• Share on label data with HCPs, discussing all aspects of the data in a scientific, objective and balanced way.
• Act as scientific expert in the key therapeutic categories for internal stakeholders.
• Provide the Zuellig organization with an understanding of the local medical community, clinical practice trends and real or perceived gaps in current scientific knowledge and medical treatment.
• Remain abreast of the latest scientific knowledge and developments in defined domains of expertise, including by means of participation in structured Zuellig training programmed
• Attend relevant scientific congresses to gather contextualized new Zuellig and competitor

information through session attendance and HCP meetings.

• Oversight of Pharmacovigilance
• Standard Operating Procedures (SOPs)
• Compliance
• Adverse Event Reporting
• Reconciliation of Safety Data and Product Complaints
• Other task assigned.

• Advanced degree in a relevant scientific field (e.g., MD, PharmD, PhD, or equivalent).
• Minimum of 2-3 years of experience in medical affairs or related field.
• Excellent communication and presentation skills.
• Strong scientific and medical knowledge
• supporting clinical trials
• working in the healthcare industry
• Communication skills
• Collaboration and teamwork skills