Drug Safety Specialist/Non-Line Manager or Staff/Patient Safety and Pharmacovigilance (Shinagawa, Japan, Tokyo)
We couldn't confirm this posting on Boehringer Ingelheim's site in our latest checks -- see current similar openings below.
About this opportunity
Basic Purpose of Job
Manage case processing activities for Nippon Boehringer Ingelheim’s investigational and marketed products including case submission to Global Patient Safety and Pharmacovigilance (PSPV) and PMDA according to Boehringer Ingelheim (BI)’s internal procedure and local regulation.
Conduct safety risk management activities, prepare and submit periodic safety reports and develop and maintain the safety part of local package inserts for the assigned compounds ensuring compliance with BI’s internal procedures and local regulation
Contribute to local asset team as an expert of benefit risk of the assigned compounds.
Accountabilities
Conduct case processing activities and case submission to Global Case Management and PMDA within reporting timeline
Related performance indicators: In time Individual Case Safety Report (ICSR) reporting to GPV/PMDA ≧98%
Conduct dissemination of safety information including SUSARs and IND reports to study sites/investigators in collaboration with Clinical Development Operations (CDO)
Related performance indicators: In time SUSARs/IND reports dissemination to study sites ≧98%
Set up case processing process for clinical trials including consultation with PMDA and coordination with CRO
Related performance indicators: Ensure in-time set up of case processing process
Maintain PV database including system update according to BI’s strategy and international regulation.
Related performance indicators: Ensure PV database updated and maintained
Ensure communication of local safety profile of NBI’s investigational and marketed compounds to stakeholders including Asset Benefit Risk Team (ABRT) Chair
Related performance indicators: Ensure global and local aligned risk management activities
Develop and update Japanese Risk Management Plan (J-RMP) in close collaboration with ABRT Chair and ensure assessment of local safety profile of Nippon Boehringer Ingelheim’s products
Related performance indicators: Ensure J-RMP timeline and quality
Implement and monitor risk minimization measures as necessary for assigned products at local level, coordinate safety issues with the local management and Global PSPV
Related performance indicators: Ensure global and local aligned risk management activities
Ensure the preparation of local periodic safety reports and coordinate a review cycle with the ABRT Chair
Related performance indicators: Ensure local periodic report preparation in time and provide qualified documents
Establish and support local inspection readiness, participate in PSPV audits and PV/GPSP inspections as required and contribute to CAPA processes as appropriate
Related performance indicators: Ensure local inspection readiness
Prepare and review SOPs and WIs and Collaborate with other teams on safety related processes
Related performance indicators: 'Ensure SOPs, WIs and KMEDs satisfying Corporate SOPs and local regulations
Coordinate revision of J-PIs (Japanese Package Inserts) according to CCDSs (Company Core Data Sheets) which Boehringer Ingelheim Corporate develops to harmonize J-PIs with global safety information
Related performance indicators: Ensure CCDS compliance in a timely manner
Take necessary measures, such as the revision of J-PIs, to ensure patient safety based on the requests/ instructions from the authorities (MHLW, PMDA), and provide safety information to the medical institutions adequately
Related performance indicators: Ensure J-PI timeline and quality
Plan and report for “Early Post-marketing Phase Vigilance” (EPPV) and safety risk communication
Related performance indicators: Ensure quality of EPPV activities and risk communication
Regulatory and/or organizational requirements
Knowledge of local and international PV regulation
Knowledge of local and international study
Interfaces
Global Patient Safety & Pharmacovigilance, Clinical Development and Medical Affairs, Clinical Development Operations, Regulatory Affairs, Experimental Medicine, Commercial Quality, Marketing, Sales, Marketing Supervisor General, Medical Director
Job Expertise
TA experience in research or industry setting
3+years’ experience in pharmacovigilance
Job Impact
Conduct and Establish internal/external collaborations by sharing best practices
Minimum Education / Degree requirements
Bachelors Degree
Required capabilities (Skills, Experience, Competencies)
Excellent command of English language
Evaluation of safety information including individual case safety reports
Proactive and assertive attitude
Team- and networker
Job details
How this role compares
Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.
We currently track 36 comparable Manager Pharmacovigilance roles across 21 biopharma companies.
Salary context
3 of 36 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 36 comparable roles
+ 11 more countries
Seniority mix
36 of 36 peers have a known seniority level
Therapeutic area mix
1 of 36 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Currently open similar roles
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.