Location: Barcelona, Spain (on-site) - 3 days/week working from the office.
At AstraZeneca
,
Requirements
in
safety programs
,
spanning
the entire life cycle of drug
development
and
peri-
/post-
submission.
O
ur Scientists and Physicians
play a
strategic
role
in develop
ing our vaccines & medicines
and the
safety
science
of the
prog
r
ams
.
AstraZeneca
’
s pipeline
includes
n
ovel combinations and modalities
,
provides a
n
intellectual challenge to the safety teams
, requiring
a
broad portfolio
and scientific
management approach to projects.
Our
teams
’
experience develops as our portfolio
does.
We are looking for
a
n Associate Director, Patient Safety (PS)
Scientist to join our Global Patient Safety V&I team. Work
ing
in the Vaccines & Immune Therapies Therapeutic Area.
In this exciting and challenging role, you will work collaboratively with the Global Safety Physician (GSP) and other PV Scientists
and physicians
. You will play
a role
supporting
the safety
strategy and
requirements for your assigned project(s)
. Your
ability to work collaboratively
will facilitate
cross-functional interactions
with colleagues from across AstraZeneca, including counterparts within Clinical Project Teams, Global Regulatory Affairs, and Global Commercial teams.
As
a
n Associate Director, PS Scientist
,
you will
be involved
in
aggregating
,
reviewing,
analyzing
and
interpreting
safety-related
data
to
generate
information
to
support
safety decision-making by prescribers, patients and payers, with the
ultimate goal
of protecting
patients.
Y
ou will apply your
PV
and scientific
, knowledge and skills
to
deliver
all aspects of
safety
documentation
,
including
authoring and / or providing
strategic safety input
to
regulatory
documents,
e.g.,
regulatory reports
,
health authority
responses
and
the
safety content of
marketing authorization applications
.
Patient Safety sits within the Chief Medical Office, where we have a crucial role to play.
This is an exciting period for us, as well as for those poised to join us.
Our strategy and ability to transform our
medicines
portfolio means we have a
drug-development
pipeline that presents incredible opportunities to push the boundaries of science to deliver life-changing medicines.
Faced with complex disease challenges,
we focus
on exceptional performance to drive the best and most transformative
development
programs ever.
A Bachelor’s in sciences/pharmacy/nursing degree
or related field
with a minimum of 3 years of experience or an advanced degree with 2 plus years of relevant experience
Patient Safety and/or Clinical/Drug Development
demonstrable
experience working in safety &/or scientific activities in at least 3 of the following areas:
Clinical drug development (Early and/or Late Phase
:
develop &
deliver
program level safety strategy, including proactive risk identification & mitigation planning)
​
​
Post-Marketing Surveillance
(including signal detection & evaluation)
​
MAA/BLA submissions
(preparation and authoring of the safety related aspects of the Common Technical Document)
Periodic
Safety
Reports
(
deliver
strategy, preparation and authoring)
Risk Management Plans (
deliver
strategy, preparation and authoring
)
Governance board interactions
and communication
across a range of activities
Good
knowledge of PV regulations
Demonstrated ability to handle more than one
activity
simultaneously, prioritizing well and recognizing key issues
Ability
to
work effectively in an advanced matrix structure
Fluent in written and verbal English
Preferred Requirements
MSc/PhD/PharmD in scientific discipline
U
nderstanding of epidemiology
Employer of Choice
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.
We offer a competitive Total Reward program including a market driven base salary, bonus and
long term
incentive. We also provide a generous paid time off program and a comprehensive benefits package!
AstraZeneca aligns with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
Date Posted
23-abr-2026
Closing Date
12-may-2026
AstraZeneca embraces diversity and equality of opportunity. Â We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. Â We believe that the more inclusive we are, the better our work will be. Â We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. Â We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.