Are you passionate about data integrity, clinical research, and driving excellence through innovation? Join our
Inscríbase (haciendo clic en el botón correspondiente) después de revisar toda la información relacionada con el trabajo a continuación.
Biometry team at BCCC
and help shape the future of data management in clinical studies.
About the Role
As a
Clinical Data Manager, you will play a key role in ensuring the
accuracy, integrity, and compliance
of clinical study data. You'll collaborate across departments to design and validate eCRFs, manage databases, and support high-quality data-driven decision-making within our organization.
You'll also take ownership of developing and maintaining efficient data systems, implementing quality improvements, and ensuring compliance with
GCP, data governance, and privacy regulations .
Key Responsibilities
Ensure
data accuracy, integrity, and regulatory compliance
across all clinical projects.
Monitor data quality, identify and resolve data issues, and propose continuous improvements.
Create
reports, dashboards, and data visualizations
for leadership insights.
Program and validate
eCRFs in EDC systems ; develop eCRF specifications and completion guidelines.
Support data cleaning, database maintenance, and
database lock and close-out
processes.
Encode medical terms (MedDRA, ICD, ATC, etc.) and define edit check specifications.
Collaborate closely with cross-functional teams within the
Operations area .
Provide ongoing
training and support
to staff on data systems and best practices.
Ensure
data accuracy, integrity, and regulatory compliance
across all clinical projects.
Monitor data quality, identify and resolve data issues, and propose continuous improvements.
Create
reports, dashboards, and data visualizations
for leadership insights.
Program and validate
eCRFs in EDC systems ; develop eCRF specifications and completion guidelines.
Support data cleaning, database maintenance, and
database lock and close-out
processes.
Encode medical terms (MedDRA, ICD, ATC, etc.) and define edit check specifications.
Collaborate closely with cross-functional teams within the
Operations area .
Provide ongoing
training and support
to staff on data systems and best practices.
Required Qualifications
Bachelor's or Master's degree in Biostatistics, Statistics, Mathematics,
Data Science, or a related field
At least
2 years of experience
in clinical data management or statistics—preferably in the
pharmaceutical or CRO industry .
Solid understanding of
Good Clinical Practice (GCP), data governance, data quality, and
data protection regulations .
Experience with
medical coding
using regulatory dictionaries.
Advanced English level
(spoken and written).
Core Competencies & Skills
Strong
organizational, analytical, and problem-solving
abilities.
Excellent
communication, collaboration, and reporting
skills.
Project management
capabilities with high attention to detail.
Proficiency in
Microsoft Office tools
and familiarity with EDC systems.
Committed to
quality, continuous improvement, and compliance .
Working conditions
Full time position
Offices located in Barcelona
Hybrid work
Competitive salary
Exclusive employee discount club, giving you special benefits and discounts across a wide range of products and services.
Starting date of the contract: November/December 2025
Why Join Us?