Maintain a good working knowledge of regulations, policies and
guidelines applicable to the role of data management and the
conduct of clinical studies within the company to support
submission efforts to regulatory agencies.
Contributes to all aspects of data management tasks from clinical
trial preparation to close out of study utilizing paper and or
electronic format. Follow defined regulations and internal
procedures to achieve high quality and accurate clinical data for
As an employee of Boehringer Ingelheim, you will actively
contribute to the discovery, development and delivery of our
products to our patients and customers. Our global presence
provides opportunity for all employees to collaborate
internationally, offering visibility and opportunity to directly
contribute to the companies' success. We realize that our strength
and competitive advantage lie with our people. We support our
employees in a number of ways to foster a healthy working
environment, meaningful work, diversity and inclusion, mobility,
networking and work-life balance. Our competitive compensation and
benefit programs reflect Boehringer Ingelheim's high regard for our
Documentation of clinical data management tasks in clinical studies
according to GCP.
Current knowledge in Clinical Data Management trends related to
Best Practice from a technical and compliance
Contribute to database edit checks and query specifications
development, to ensure quality output.
Contribute to harmonization of data exchange with external
cooperations, e.g. laboratories.
Contribute to provide written spec for loading non CRF data into
the database in collaboration with programmers.
Control that requirements for data transfer and integration with
other systems are available.
Contribute to the preparation of statistical data sets in the
predefined format for the statistician.
Contributing to creation of Data Management Planning documentation
including but not limited to data entry instruction and Data
Oversee incoming CRFs and DCFs for completion, consistency and
clarity. Managing and tracking CRF flow including scanning as
Ensure clinical project time lines are met with acceptable quality
metrics, and provide appropriate communication of status, issues
The selected candidate will be hired at the appropriate level
based on experience and education level.
Clinical Data Coordinator I
Bachelors’ degree from
an accredited institution in Biology and/or Computer Science
to two (2) years of direct experience in Pharmaceutical industry or
to support multiple (5-10) clinical studies.
degree of detail orientation and excellent written and verbal
Clinical Data Coordinator
Bachelor's degree from an accredited institution with a major focus
in Data Management, Life Science, Computer Science or Math (for
Germany Master degree or equivalent clinical data management
Two to four (2-4) years of direct experience in Clinical Data
Management or related field.
Ability to support/contribute multiple (1-5) clinical
Knowledge and experience in and continuing education of clinical
trial designs, data standards, clinical trial conduct and
methodology VICH regulations, Good Clinical Practice (GCP), major
regulatory authorities and relevant directives/regulations) are
Knowledge of Best Practice in the field of clinical data management
including some knowledge in PL, SQL and statistics is
High degree of detail orientation and excellent written and verbal
Coordinates own work and performs site-specific tasks with
Professional customer focus approach.
Responsible for the clinical trial database and the data collected
within a trial/study and/or for the identification, detection and
assessment of risks in a clinical trial under the supervision of a
Sr. CDM or Principal CDM.
Must be legally authorized to work in the United States without
Must be willing to take a drug test and post-offer physical (if
Must be 18 years of age or older
Boehringer Ingelheim we create value through innovation with one
clear goal\: to improve the lives of patients. We develop
breakthrough therapies and innovative healthcare solutions in areas
of unmet medical need for both humans and animals. As a family
owned company we focus on long term performance. We are
powered by 50.000 employees globally who nurture a diverse,
collaborative and inclusive culture. Learning and development
for all employees is key because your growth is our
Want to learn more? Visit boehringer-ingelheim.com and
join us in our effort to make more health.
Ingelheim is an equal opportunity global employer who takes pride
in maintaining a diverse and inclusive culture. We embrace
diversity of perspectives and strive for an inclusive environment,
which benefits our employees, patients and communities. All
qualified applicants will receive consideration for employment
without regard to a person’s actual or perceived race, including
natural hairstyles, hair texture and protective hairstyles; color;
creed; religion; national origin; age; ancestry; citizenship
status, marital status; gender, gender identity or expression;
sexual orientation, mental, physical or intellectual disability,
veteran status; pregnancy, childbirth or related medical condition;
genetic information (including the refusal to submit to genetic
testing) or any other class or characteristic protected by