Associate Director Biostatistics
About this opportunity
Career Category
Clinical Development
Job Description
What you will do
Amgen is expanding its global Biostatistics capabilities, with Amgen Taiwan playing a key role in integrated delivery and functional leadership. As Associate Director, Biostatistics, you will contribute statistical strategy, operational execution, and scientific leadership across Amgen’s clinical programs. You will oversee statistical contributions to clinical trials, lead study teams, and support regulatory and reimbursement submissions, while mentoring and managing statisticians. Throughcross-country and cross-functional collaborations, you will have the opportunity to contribute to innovative technologies that enhance scientific and/or operational efficiencies in drug development.
This role provides both hands-on technical leadership and managerial responsibility, ensuring quality, compliance, and innovation in biostatistical delivery aligned with Amgen’s global clinical development strategy.
Responsibilities:
Provide sound statistical guidance to clinical development, reimbursement, and medical affairs.
Oversee statistical contributions to protocols, randomization specifications, statistical analysis plans (SAPs), clinical study reports (CSRs), and key trial documents.
Ensure alignment of study design and analysis with scientific rigor, regulatory requirements, and Amgen policies.
Collaborate cross-functionally with global teams to deliver high-quality analyses, publications, and regulatory filings.
Contribute to innovative trial designs, advanced methodologies, and process improvement initiatives.
Provide sound statistical guidance to clinical development, reimbursement, and medical affairs.
Oversee statistical contributions to protocols, randomization specifications, statistical analysis plans (SAPs), clinical study reports (CSRs), and key trial documents.
Ensure alignment of study design and analysis with scientific rigor, regulatory requirements, and Amgen policies.
Collaborate cross-functionally with global teams to deliver high-quality analyses, publications, and regulatory filings.
Contribute to innovative trial designs, advanced methodologies, and process improvement initiatives.
Execute biostatistical strategies across the product lifecycle, from early development through post-marketing.
Provide consultancy and training to colleagues across R&D.
Support governance of outsourced statistical activities, ensuring adherence to Amgen standards and regulatory compliance.
Represent Biostatistics in cross-functional and external interactions (e.g., with regulatory agencies, investigators, or data monitoring committees).
Drive technology adoption leveraging AI capabilities to streamline statistician’s work
Basic Qualifications
Doctorate in Statistics/Biostatistics (or related subject with high statistical content) with at least 5 years of post-graduate statistical experience in the pharmaceutical industry or medical research, OR
Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with at least 8 years of post-graduate statistical experience in the pharmaceutical industry or medical research.
Successful managerial experience of a group of statisticians and statistical programmers.
Preferred Skills
Doctorate in Statistics/Biostatistics (or related subject such as data science, engineering with high statistical content) with at least 7 years of post-graduate statistical experience in the pharmaceutical industry or medical research, OR
Master’s degree in Statistics/Biostatistics (or related subject such as data science, engineering with high statistical content) with at least 10 years of post-graduate statistical experience in the pharmaceutical industry or medical research.
Experience developing interactive or advanced visualizations to enhance interpretation of clinical trial data is a plus. Familiarity with R or Python is preferred.
Prior experience in growing a successful team of statisticians within Clinical Development
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Job details
How this role compares
Computed from every other active Clinical Development role in our database, not just this employer's listings.
We currently track 384 comparable Associate Director Clinical Development roles across 71 biopharma companies.
Salary context
103 of 384 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 384 comparable roles
+ 23 more countries
Seniority mix
384 of 384 peers have a known seniority level
Therapeutic area mix
42 of 384 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.