Job Title:
Clinical Programmer I
Location:
Barcelona
At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person.
Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices
3 days a week
. Our head office is purposely designed with collaboration in mind, providing space where teams can come together to strategize, brainstorm and connect on key projects.
Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we're taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention.
Introduction to Role:
As a Clinical Data Manager I, you will support the delivery of high-quality clinical data for assigned studies and indications across different Data Management sourcing models. Working under the guidance of an experienced Data Management Lead, you will contribute to a variety of data management activities while ensuring data quality and operational excellence.
You will collaborate with integral study teams and external partners, including CRAs and data providers, to support day-to-day clinical data management activities. This role offers an excellent opportunity to develop your expertise and contribute to the successful execution of clinical studies in a global environment.
Accountabilities:
Assist
with
Study
level
CDM
administrative
support
based on
the
relevant
model
and
DM
Vendor.
This
may
include but is not limited to activities related to the study start up,



conduct and closeout phases. (i.e., documentation review and/or creation, User Access Testing, query management, data cleaning and reviews, third party data reconciliation in accordance with the project study model, KPIs and timelines.).
Day
to
day
responsibilities
may
include
but
are
not
limited
to:
-
Study status reporting to the
relevant clinical study team
members, (e.g., provide data to
clinical
teams for
performing
medical
and
clinical
reviews,
coordination
of
instream
data
review, lab
data
review,
etc.); -
Collaboration
with
Data
Management
Vendor
regarding
upcoming
deliverables
and
milestone achievements (i.e., snapshots, interim, and migrations);
-
Oversight
of
the
data
quality,
documentation
quality,
and
types
of
these
deliverables
and
milestones.
Support
DM
Delivery
Leads
to
maintain
CDM
specified
systems
and
types
of
deliverables,
milestone
achievements, risks and mitigations and data transfer agreements, and other study administrative needs.
Support
DM
Delivery
Leads
in
oversight
of
Trial
Master
File
compliance
for
audit
readiness.
May
include
activities related to study expected document Lists and quality compliance checks.
Support
DM
Delivery
Leads
in
User
Acceptance
Testing
of
internal
and
external
electronic
Data
Capture
systems
as
required.
Provides
support
to
the
resolution
of
issues
related
to Clinical
Data
Management
deliverables and
inputting
ideas to help resolve issues and contribute to continuous improvement.
Performs
any
CDM
related
ad-hoc
requests
as
requested
by




the
DM
Leads.
Essential Skills/Experience:
University
or
college
degree
in
the
life
sciences
or related subject, pharmacy, nursing or equivalent relevant degree
.
Languages:
Fluent
English
(oral
and
written)
.
Attention
to
detail
to
ensure
quality
.
Good
verbal
and
written
skills.
Ability
to
work
flexibly
on
simultaneous
projects
and proactively manage time to meet own deadlines.
Strong interpersonal skills and proven ability to communicate
effectively
in
a
global
environment.
Desirable Skills/Experience:
Basic understanding of clinical trials methodology,
Clinical
Data
Management, GCP and medical terminology.
Where can I find out more?
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Are you interested in working at AZ, apply today!
AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing
******
.
Date Posted
12-jun-****
Closing Date
25-jun-****
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 comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

📌 Clinical Programmer I (Laza)
🏢 AstraZeneca
📍 Laza