PHARMACOVIGILANCE EXECUTIVE ( CẢNH GIÁC DƯỢC)

Main responsibilities
Salary: Negotiation
Working hours: Mon – Fri
Period: 1 year contract, full- time
Field: Patient Safety & Pharmacovigilance (PSPV)
Work Location: District 1, HCMC
• Is responsible for Vietnam – Cambodia – Laos
• Replaces the CSH in most of his/her tasks when he/she is out of the office,
including acting as local PV contact for the authorities and being accountable
for PV inspections
• Supports the CSH in ensuring that local PV activities are performed in
market in the assigned countries
compliance with the PSPV policies, as well as global, regional and local PV
regulations to warrant safe and appropriate use of Sanofi products on the
• Supports the CSH in ensuring establishment and maintenance of a robust and
efficient local PV system by ensuring the availability and implementation of
proper systems/procedures, tools and training
• Serves as the local PV contact for the local authorities and acts as the local
legislation (this role can be delegated as needed)
Responsible Person for Pharmacovigilance (RPP) where applicable per country
Requirements:
Experience:
• Experience with pharmacovigilance systems and safety- related product
recommended
management in both clinical development and marketed products is highly
• A minimum of experience in either pharmacovigilance or regulatory or quality
r medical or clinical development is necessary
• Experience on required standards for high quality safety relevant documents,
Manpower Vietnam – Job Description
g. RMP, PBRER is a plus
• Experience with Regulatory Agency interactions
Soft skills:
• Leadership, able to create networks and to collaborate in an international crossfunctional environment
• Interpersonal skills of diplomacy and team player dynamics; knowledge of and
respect for cultural differences; professionalism and mediation are important
• Demonstrate problem solving skills, sense of urgency, especially with respect to
enforcing safety rules and global procedures as described in QDs, Operational
Manuals and Guidance documents. Capacity to work under pressure
• Ability to work in international and transversal teams.
Technical skills:
• Able to evaluate & manage safety signals and define risk management activities
• Robust knowledge of pharmacovigilance systems & regulations
• Sufficient ability to interpret clinical data including safety data
Education:
• Advanced health care discipline degree (MD, PharmD, PhD, Master of Science,
) or equivalent qualification
Languages:
• Professional English language proficiency

Cập nhật gần nhất lúc: 2025-08-17 21:05:02