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This position was posted on May 7, 2026 and is likely no longer accepting applications. We've kept it here for historical reference. Check out the similar jobs below!
Job Overview
Location
BogotĂ
Job Type
Full-time
Category
Product Management
Date Posted
May 7, 2026
Full Job Description
đź“‹ Description
- • The Associate Clinical Data Manager (ACDM) role is critical to ensuring the quality, integrity, and compliance of clinical trial data sourced from external vendors across global studies, directly supporting the success of clinical development programs.
- • Day to day, the ACDM will support end-to-end acquisition of third-party clinical data, collaborate with external vendors on timelines and issue resolution, monitor data deliverables for risks and inconsistencies, partner with cross-functional study teams, represent ACDM activities in meetings and audits, and contribute to process improvements and data integration initiatives.
- • Fortrea Holdings Inc. is a global leader in clinical research services, operating in a dynamic, innovation-driven environment focused on advancing therapeutic development through rigorous data standards and global collaboration.
- • In this role, you will deepen your expertise in clinical data management, gain hands-on experience with CDISC standards (SDTM, ADaM), ICH-GCP, and global regulatory requirements, while developing leadership in vendor coordination, data governance, and process optimization—positioning you for advancement into senior data management or clinical operations roles.
🏖️ Benefits
- • Exposure to multiple therapeutic areas and development phases
- • Collaboration with global teams and innovative data technologies
- • Opportunity to make a meaningful impact on clinical development programs
- • Home-based position based in Colombia (mandatory)
- • Professional growth through process improvement and data integration initiatives
Skills & Technologies
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About Fortrea Holdings Inc.
Fortrea is a global contract research organization spun out from LabCorp in 2023 to provide drug development services across Phases I-IV. It offers clinical trial management, patient access solutions, regulatory consulting, and commercialization support to biopharmaceutical, medical device, and diagnostic clients. The company operates in more than 90 countries with 19,000 employees, leveraging therapeutic expertise in oncology, rare diseases, neuroscience, and other complex areas to accelerate therapies from lab to market while prioritizing patient experience and data-driven insights.
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