Sr. Manager/Associate Director, Statistical Programming
Posted on: June 7, 2021
We believe it's possible to have a profound impact on bending
the cost curve in healthcare by building a pipeline of innovative
medicines and bringing them to market at dramatically lower
Robert Forrester CXO
EQRx believes responsibility can be revolutionary. Want to make
a difference while advancing your career? Come join a team that is
working towards our bold mission of developing innovative medicines
at radically low prices to help people get the medicines they
What You'll Do
As the Sr. Manager/AD of Statistical Programming you will lead
the programming activities within a therapeutic project at EQRx.
You will ensure the quality of deliverables by consistently
applying analysis and reporting standards and driving compliance
with regulatory requirements. You will develop clear and robust
programming specifications for internal and external programming
work and review planning documents (e.g. statistical analysis
plans, data presentation plans, data review plans) to ensure
clarity, integrity and compliance with requirements and standards.
You will build and manage a regulatory compliant computing
environment and statistical programming SOPs. You will interact
with other internal functions (biostatistics, regulatory and
medical writing) to define and produce user-defined statistical
reports (e.g., ad hoc requests). You will also oversee internal and
external programming projects within a therapeutic project.
The Impact You Will Have
Our mission is to make innovative drugs that are affordable and
accessible. This is not your standard statistical programming
position. We are doing things differently here than how it is
normally done, and this role is no exception. We are building our
infrastructure and processes from the ground up, and at EQRx, you
will be encouraged to thoughtfully integrate novel technologies in
support of our vision.
- You have a graduate degree in statistics, biostatistics,
mathematics, computer science or equivalent experience.
- You have 8+ years of clinical/statistical programming
experience within pharmaceutical clinical development with
experience that includes leading programming efforts to support
regulatory filings (e.g., US, EU, Japan) with at least 2 years of
experience in overseeing technical professionals in a regulated
- You have extensive knowledge of SAS software (i.e., Base, Stat
components) and general computing techniques and a knowledge of R
or other statistical software packages.
- You have significant knowledge of the drug development process,
clinical trial methodology, CDISC standards, statistics, and
relevant regulatory requirements for drug approval.
- You have submission programming experience in late phase
- You can participate and work effectively on multiple
- You understand relationships are key and have strong
- You are a great communicator. If you can speak Mandarin that is
- Teams love working with you and you are someone who takes pride
in mentoring and supporting the careers of others.
- You can thrive in a smaller company environment and love the
pace of a true startup.
- You're a team player who is willing to roll-up your sleeves and
get the job done.
Are you bold enough?
Your work should matter and allow you the freedom to be 100%
you. We spend too much time and effort in our career to not feel
excited and proud about what we do and who we do it with. In other
words, your career is too important for your next move to be just
another job, so let's work together to change the world and bring
affordable medicines to all patients.
We aren't about a bunch of empty slogans on a wall or words on a
coffee cup - you can find that in lots of places. We are a culture
of individuals with diverse backgrounds and personalities.
Keywords: EQRx, Cambridge , Sr. Manager/Associate Director, Statistical Programming, Other , Cambridge, Massachusetts
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