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Job ID : 1517821
Date Updated :
January 28th, 2025
PR/094727 | Safety Physician
| Location | Singapore, Singapore |
| Job Type | Permanent Full-time |
| Salary | Negotiable, based on experience |
Job Description
COMPANY OVERVIEW
The client, a global pharmaceutical company is now seeking a Safety Physician to be part of their Global Patient Safety department contributing greatly to achieving good Pharmacovigilance compliance in the region and globally. The incumbent will be responsible in performing medical safety tasks to ensure the safety of patients taking their drugs.
The client, a global pharmaceutical company is now seeking a Safety Physician to be part of their Global Patient Safety department contributing greatly to achieving good Pharmacovigilance compliance in the region and globally. The incumbent will be responsible in performing medical safety tasks to ensure the safety of patients taking their drugs.
JOB RESPONSIBILITIES
- You are responsible for the medical review of individual case safety reports (ICSRs) for all products.
- Accountable for medical evaluation/interpretation of individual safety reports and aggregate safety data of products assigned including signal detection and evaluation, regulatory safety reports (PSUR, DSUR, PBRER), and ad hoc safety review/assessments.
- You are expected to timely communicate potential safety signals to line management.
- Adhere to relevant corporate and Global Pharmacovigilance Standard Operating Procedures and Working Instructions.
- Perform good quality and timely handling of single case reports (incl. medical review, qualified follow-up in ARISg Pharmacovigilance Database).
- Keeping up to date on and communicating information from various sources in pharmacovigilance and the therapeutic areas.
- Contribute to knowledge and information-sharing within/across Therapeutic Groups and Global Pharmacovigilance.
- Participate in relevant cross-functional/organizational projects
- Participate in the preparation, review, and maintenance of Global Pharmacovigilance Standard Operating Procedures, Working Instructions, and Templates.
JOB REQUIREMENTS
- A medical degree with at least 6 years of clinical practice. Pharmaceutical industry experience is high preferred. A combination of experience and/or education will be taken into consideration.
- Strong clinical background. Specialization in Neurology/Psychiatry therapeutic area will be an added advantage.
- Familiar with electronic safety databases (ARISg, ARGUS), coding dictionaries (MedDRA, DS Navigator, Medidata Coder) is preferred.
- Strong and effective communication and time management skills
- Good drug information research skills and the ability to conduct online research
- Meticulous at work, self-motivated
- Good team player, and at the same time able to work independently
Apply online or feel free to contact me directly for more information about this opportunity. Due to the high volume of applicants, we regret to inform that only shortlisted candidates will be notified. Thank you for your understanding.
EA JAC Recruitment Pte. Ltd.
EA Licence: 90C3026
EA Personnel: R1109147
EA Personnel Name: Noor Suliana Liza Binte Ab Lateb
#LI-JACSG
#countrysingapore
EA JAC Recruitment Pte. Ltd.
EA Licence: 90C3026
EA Personnel: R1109147
EA Personnel Name: Noor Suliana Liza Binte Ab Lateb
#LI-JACSG
#countrysingapore
General Requirements
| Minimum Experience Level | Over 3 years |
| Career Level | Mid Career |
| Minimum English Level | Business Level |
| Minimum Japanese Level | Business Level |
| Minimum Education Level | Associate Degree/Diploma |
| Visa Status | No permission to work in Japan required |
Job Location
- Singapore, Singapore
Work Conditions
| Job Type | Permanent Full-time |
| Salary | Negotiable, based on experience |
| Industry | Healthcare, Nursing |
Job Category
- Other > Other
