- 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