(Sr) Patient Safety Specialist (Taipei, Taiwan, TW)
About this opportunity
Main job tasks
1. Conduct drug safety surveillance and adverse reaction assessments
- Monitor and evaluate adverse reaction reports to determine relatedness to Novo Nordisk products
- Perform follow-up activities to ensure comprehensive safety data collection
2. Ensure compliance with regulatory requirements
- Adhere to governmental regulations and company policies in all safety pharmacovigilance activities
- Support the resolution of legal liabilities related to drug safety
3. Provide safety support for clinical development teams
- Collaborate with clinical teams to address safety concerns during product development
- Offer expert advice on safety strategies and risk mitigation
4. Contribute to safety signal detection and risk management
- Analyse trends and identify potential safety signals for products throughout their lifecycle
- Participate in risk management assessments to ensure patient safety
5. Oversee safety in clinical trials and post-marketing programmes
- Monitor safety data from clinical trials and post-marketing activities and monitor PV Agreement suppliers through periodic compliance checks in scope of the PV Agreement
- Ensure robust safety oversight and reporting mechanisms are in place
Qualifications:
Education
-Master’s degree in Pharmacy, Life Sciences, or a related field is preferred.
Experience
- 1- 5 years of experience in pharmacovigilance or drug safety is preferred .
-Familiarity with clinical trials and post-marketing safety programmes.
-With the pharmaceutical industry experience is preferred.
- Good command of written and spoken English. Professional working proficiency in English, with the ability to communicate effectively with stakeholders.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
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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 31 comparable Senior Pharmacovigilance roles across 20 biopharma companies.
Salary context
9 of 31 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 31 comparable roles
+ 8 more countries
Seniority mix
31 of 31 peers have a known seniority level
Therapeutic area mix
3 of 31 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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.
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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.