Data Manager

As a 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.

• 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.

• 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).

• 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.

• 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

At BCCC, you’ll be part of a collaborative and innovative team that values precision, integrity, and scientific excellence. We offer a dynamic work environment where your expertise will directly contribute to the success of meaningful clinical studies impacting patients worldwide.