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求人ID : 1517821
更新日 :
2025年01月28日
PR/094727 | Safety Physician
| 勤務地 | シンガポール, Singapore |
| 雇用形態 | 正社員 |
| 給与 | 経験考慮の上、応相談 |
募集要項
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
応募必要条件
| 職務経験 | 3年以上 |
| キャリアレベル | 中途経験者レベル |
| 英語レベル | ビジネス会話レベル |
| 日本語レベル | ビジネス会話レベル |
| 最終学歴 | 短大卒： 準学士号 |
| 現在のビザ | 日本での就労許可は必要ありません |
勤務地
- シンガポール, Singapore
労働条件
| 雇用形態 | 正社員 |
| 給与 | 経験考慮の上、応相談 |
| 業種 | 福祉・介護 |
職種
- その他 > その他
