Biostatistical Programming Senior Associate
About this opportunity
Career Category
Clinical Development
Job Description
Sr Associate Biostatistical Programming
The Biostatistical Programming Senior Associate will work in Amgen's Global Randomization and Blinding (GRB) organization
Responsibilities include:
Creating and delivering Participant and Investigational Product (IP) randomization lists meeting specifications per randomization requests. Perform the duties of a Study Randomizer as needed
Write and validate SAS programs to verify randomization assignments and dose decisions performed by an Interactive Response Technology (IRT) system throughout the conduct of a clinical trial.
Function as a study programmer to manage IRT data transfer activities
Act as a gatekeeper for IRT data transfers into Amgen’s secure File Transfer Protocol (sFTP) locations.
Understand and execute both department and study level macros and utilities
Ongoing verification of electronic systems used to execute randomization schedules and dosing algorithms
Ensuring procedures are followed to maintain the study blind per Amgen Study Operating Procedures (SOPs) throughout the lifecycle of a study
Maintaining accurate and complete documentation of randomization and blinding activities and communications
Assist with study and systems audits by internal and external bodies and respond to audit questions and findings
Participate in the development and review of GRB policies, manuals, SOPs and other controlled documents
Cross functional training and presentations
Knowledge:
Biostatistical programming using SAS version 8.2 and higher or other programming languages (e.g. R or Python)
Understanding of computer operating systems, including UNIX, preferred
Project planning and management
Basic understanding of IRT systems preferred.
Drug development processes and operations
Basic Qualifications:
BA/BSc or higher degree in biostatistics, statistics, mathematics, computer science, or related subject. At least four years of statistical programming experience in relevant career statistical programming experience in a clinical development environment.
Preferred Qualifications :
MSc or higher degree in statistics, biostatistics, mathematics, or related subject
Six years of clinical research programming experience
Drug development in related industries
Project planning
Process improvement participation
Team participation and effectiveness
.
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 186 comparable Senior Clinical Development roles across 34 biopharma companies.
Salary context
41 of 186 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 186 comparable roles
+ 17 more countries
Seniority mix
186 of 186 peers have a known seniority level
Therapeutic area mix
21 of 186 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.
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.