Senior Manager, Clinical Data Management

Role: Senior Manager, Clinical Data Management overseeing data activities in biopharma clinical trials. Responsibilities: ensure accuracy and consistency of databases, develop and supervise data management processes, coordinate with CROs and internal teams on data collection, review, and database lock activities; contribute to SOPs and quality compliance; manage external vendor interactions and support regulatory documentation. Requirements: bachelor’s degree in science or healthcare; 7+ years in clinical data management within pharma, biotech, or CRO settings; experience with data systems like Medidata RAVE, IWRS, and relational databases; knowledge of ICH, 21 CFR Part 11, FDA, CDISC, SDTM, and MedDRA; strong communication, project management, and problem-solving skills. Preferred: proficiency in data visualization tools and regulatory standards. High-Value: focus on clinical trial data for biopharma development, with up to 20% travel; involved in multi-phase trials in a fast-paced, matrixed environment.