Associate Manager/Manager, PV (Shanghai, China)
About this opportunity
About Human Pharmaceutical Business
With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs of the patients we serve in the following key areas of interest: cardiovascular, respiratory, metabolic diseases, immunology, oncology and central nervous system. In the future, we will accelerate the launch of more than 10 innovative medicines to meet the demand of Chinese patients.
Responsibilities
Provide scientific inputs from safety perspectives in key milestones across asset lifecycle including but not limited to the briefing book, IB, CTP, CTR, local label, ICSRs, etc.
Lead the local RMP strategy and ensure on-time and high-quality local RMP preparation, implementation and evaluation according to local regulatory requirements.
Generate local safety reports to Health Authority per regulations like safety summary for license renewal, fatal/cluster case investigation reports, etc.
Review the local safety with summary per requirements and keep necessary communication with relevant stakeholders.
Provide scientific inputs from safety perspective on the post-marketing studies (e.g. ONIS, IIS, ECR) and contribute to the development and implementation for the local PASS per local regulations
Deliver PV knowledge or asset safety profile training to internal and external customers as needed.
Support LPSL on maintenance of local PV system and contributes to the PV Quality system
Qualifications
Master’s degree or above in clinical medicine
3+ years of pharmaceutical industry/hospital experience, pharmacovigilance or clinical development/medical affairs role is a plus
Excellent medical judgment and scientific analysis skills
Strong communication and influencing skills
Cross-functional collaboration
Strategic thinking and project management
Risk assessment capabilities
Good Command of English and Chinese
]]>
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 29 comparable Manager Pharmacovigilance roles across 15 biopharma companies.
Salary context
2 of 29 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 29 comparable roles
+ 8 more countries
Seniority mix
29 of 29 peers have a known seniority level
Therapeutic area mix
0 of 29 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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.