Menu
Connecting...
- Location
- Shanghai
- Salary
- Competitive Salary
- Job Type
- Permanent
- Ref
- BH-17782
- Contact
- Yin Yin Pui
- Contact email
- Email Yin
- Contact phone
- +65 6692 0751
- Posted
- 大约 3 小时 前
Industry: RNAi Therapeutic Biotech
Responsibilities:
- Monitor safety data for assigned therapeutic projects in (pre-market) clinical stages; review adverse event reports including SAEs (serious adverse events) and unexpected events
- Proactively identify safety signals, conduct benefit-risk assessments using safety data and literature available
- Ensure accurate safety data entry in pharmacovigilance databases, assist in safety report preparation
- Stay updated on global regulations landscape, collaborate with regulatory teams to ensure timely safety document submissions
- Support cross-departments collaboration on patient safety reviews and related projects.
Qualifications:
- Clinical Medicine degree (MD)
- 5 years prior experience in handling PV or patient safety in pharma / biopharma industry
- Familiar with regulatory guidelines (e.g. MAH, ICH, NMPA, FDA, etc.)
- Effective communicator with excellent analytical skills
BeathChapman Pte Ltd
Marketing Manager
- Singapore
- Competitive Salary
One of our clients who first entered Singapore back in 2023 is continuing to grow and expand across SEA and as such are looking for a Marketing Manager to join their team. You will be the sole ma...
AI Protein Scientist
- Singapore
- Competitive Salary
One of our clients who first entered Singapore back in 2023 is continuing to grow and expand across SEA and as such are looking for an AI Protein Scientist to join their team. You will be the fir...
