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FortreaPosted 2 months ago

Senior Clinical Data Manager - sponsor dedicated - oncology

On-siteMaidenhead, England, United Kingdom

Full TimeSenior LevelLarge

Job Summary

Senior Clinical Data Manager role in sponsor-dedicated department focusing on oncology; responsible for full cycle of Clinical Data Management queries, leading studies (including healthy volunteer and patient populations, multi-site, complex protocol designs), serving as main client contact, and performing hands-on CDM tasks such as eCRF creation, data cleaning, and setup-to-close-out duties. Provides CDM leadership for one or more projects, oversees vendor contracts and budgets, ensures risk management and issue escalation, mentors junior staff, and collaborates with cross-functional teams (Data Coordinators, Statistical Programmers, etc.). Requires strong client management, CRO/Pharma experience, knowledge of CDASH/SDTM standards, and understanding of trial processes, regulatory obligations, and data systems. Offers office-based or home-based work across listed countries with competitive benefits, flexible hours, and onboarding support. Fortrea is an Equal Opportunity Employer, encouraging all to apply; privacy and accommodations information provided. The role emphasizes leadership, program-level CDM delivery, and global impact in clinical trials.

Required Qualifications

  • University/college degree (life science, pharmacy or related subject preferred)
  • 8 years of combined early or late-stage DM experience with minimum 2 years direct sponsor management and at least 2 years technical mentoring experience
  • Extensive experience in clinical data management and experience leading studies in a CRO/Pharma setting
  • Understanding of RECIST criteria
  • Excellent oral and written communication and presentation skills
  • In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations
  • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies

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