Drug Safety Associate
- SINGAPORE, Singapore
- Salary negotiable
- 16 applications
- Job type: Permanent, full-time
- Date:
- Reference: 22491447
Organisation Description
The client is a global leader in the Pharmaceutical industry with strong presence in Asia Pacific. With expansion of their Pharmacovigilance and Drug Safety team, they are on the hunt for a experience Drug Safety Associate to be part of their dynamic team.
Job Description
Drug Safety Associate is directly accountable for the performing the assigned safety tasks allocated to the Shared Service Centre in a given region. Countries of focus will be Thailand, Vietnam, Indonesia, Philippines, Hong-Kong, Pakistan and potential emerging markets where the company does not have an affliate in. The tasks have to be performed in order to ensure full compliance with all global and local regulatory requirements for safety data management and reporting, communication of product-specific safety information to achieve effective safety risk mitigation and optimize the benefit-risk of all products within the company.
Person Specification
To qualify, you will have at least 3 years experience in pharmacovigilance in the pharmaceutical industry, in an affiliate setting and if possible also at corporate level. You will preferably possess strong knowledge of regional and local regulatory pharmacovigilance processes as well as knowledge of Good Clinical Practice and Good Pharmacovigilance Practice.
The client is a global leader in the Pharmaceutical industry with strong presence in Asia Pacific. With expansion of their Pharmacovigilance and Drug Safety team, they are on the hunt for a experience Drug Safety Associate to be part of their dynamic team.
Job Description
Drug Safety Associate is directly accountable for the performing the assigned safety tasks allocated to the Shared Service Centre in a given region. Countries of focus will be Thailand, Vietnam, Indonesia, Philippines, Hong-Kong, Pakistan and potential emerging markets where the company does not have an affliate in. The tasks have to be performed in order to ensure full compliance with all global and local regulatory requirements for safety data management and reporting, communication of product-specific safety information to achieve effective safety risk mitigation and optimize the benefit-risk of all products within the company.
Person Specification
To qualify, you will have at least 3 years experience in pharmacovigilance in the pharmaceutical industry, in an affiliate setting and if possible also at corporate level. You will preferably possess strong knowledge of regional and local regulatory pharmacovigilance processes as well as knowledge of Good Clinical Practice and Good Pharmacovigilance Practice.
