Pharmacovigilance - 製薬会社

Location: Tokyo
Contract Type: Permanent
Salary: ¥7000000.00 - ¥10000000.00 per annum
Specialization: Life Science (Medical Devices / Pharmaceutical / Chemical / Healthcare / Agriculture / Livestock),
Sub Specialization: PV / Safety,
Contact: Hidetoshi Sato
Reference: JO-2111-465099

※Applicants must have permission to work in Japan and required fluent ~ native level Japanese.

[Position] Pharmacovigilance
[Location] 東京都/在宅勤務制度あり
[Salary] 7〜10 million JPY ※Experiences and skills will be considered

[Company Description]

  • 世界中で事業を展開するトップクラスの企業


  • Safety Scientist is responsible for leading to execution of Pharmacovigilance activities including PMS studies of the products basically post marketing phase including re-examination properly and timely, and for ensuring the Patient's safety by To develop and maintain the Risk Management Plan of the products in Japan based on the PV activities' results and other information.
  • When the safety issue arises, lead to define the appropriate safety measurement through the communication with the related internal parties including JPV team and Global patient safety with external parties (including co-proportioned company, PMDA and MHLW etc.).
  • Managing quality Pharmacovigilance deliverables such as RMP(Revision), EPPV report, PMS report, J-PSUR and Re-examination package etc. of the assigned products/projects throughout the product's lifecycle.
  • Work on management of PMS study, EPPV and communication of Safety Assurance Measure as PV associate member.


  • Bachelor's Degree in Science or related discipline
  • Relevant safety experience or experience elsewhere in Pharmaceutical industry
  • Cross-functional project team experience
  • Thorough knowledge of the Pharmacovigilance or drug development process
  • Written and verbal communication skills
  • Scientific knowledge sufficient to understand all aspects of safety issues
  • Communication/negotiation skill
  • Leadership skill
  • Problem solution skill
  • Logical thinking
  • Understanding of PMD Act, relevant regulations, GVP/GPSP and guidelines
  • Basic knowledge of statistical analysis
  • Expertise of medical/pharmaceutical science in general
  • Business English

[Preferred Knowledge, Skills and Abilities]

  • Pharmacovigilance activities , Drug development or regulatory affairs experience in outside of Japan
  • Working with external bodies, such as co-marketing companies and advisory board members, as a leading person

Please click "apply" if you are interested in the job.
We will review your profile and contact you within five business days should we find that you satisfy the requirements of the hiring company.
Further details about the company and position will be notified at a later date.
Reference: JO-2111-465099
Seniority Level: Mid-Senior level
Job Function: Quality Assurance