Principal Data Manager
October 30
Description
• Ensure DM tasks for assigned studies are performed on time and within budget • Partner with Sponsors, clinical and statistics to develop the data collection specification • Manage in-stream data flow activities and deliver a quality database in accordance with the project plan • Lead and drive the DM team • Act as the reference point for the Sponsor from the data management perspective • Define and develop the Data Management Plan, Data Validation Plan and their annexes • Validate the database and computerized checks, including SAS listings or SAS checks • Perform timely data integration of CRF and non CRF data
Requirements
• Degree in life science, pharmaceutical, biology or related field or at least 6 years’ experience in data management field or similar in a pharmaceutical environment or equivalent • Knowledge of Data Management processes • Very Good Knowledge of pharmaceutical industry guidelines like ICH, GCP etc • Very Good Expert in one or more DM systems or processes and recognized for their expertise • Able to propose standards across studies and therapeutic areas • Proficiency in Medidata Rave or Merative Zelta • Oncology experience
Benefits
• Professional development • Global travel • Flexible work programs
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