> Markdown version of [/jobs/ext/4238739-senior-manager-data-management](https://www.wearedevelopers.com/jobs/ext/4238739-senior-manager-data-management). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Manager, Data Management - **Company:** TEVA PHARMACEUTICAL INDUSTRIES LIMITED - **Location:** West Chester, PA, United States - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Clinical Data Management, Databases, Data Cleansing, Monitoring of Systems, SAS (Software), Systems Integration, Core Data, Data Management - **Published:** October 5, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=a4457d81ce86bace ## About the Role Education Required: Bachelor's Degree or higher, or equivalent amount of combined educational and work experience is required. Exceptional candidates may be considered with less years depending on experience and education. Experience Required: Managers / Senior Managers require at least five years /seven years of data management experience in a pharmaceutical or clinical research setting. Experience in data management, systems, technical and outsourcing. Experience in directly managing/overseeing service providers is desired. Experience with computerized clinical data management systems. Strong understanding and experience with eCOA and ePRO systems and leading studies with eCOA. Experience Preferred: Knowledge of SAS and database programming, systems integration experience and understanding of CDASH and CDISC standards are preferred. Specialized or Technical Knowledge Licenses, Certifications needed: NA Functional Knowledge: See "Experience Required" Company/Industry Related Knowledge: Understanding of FDA and international regulations. Thorough understanding of the drug development process, clinical trial methodology, GCP regulations, and data management principles. Job-Specific Competencies: 1. Strong and effective oral and written communication skills and interpersonal skills. 2. Ability to work in a virtual, global and multi-cultural environment. ## Description Ensures data management activities and deliverables for area(s) of responsibility are completed in line with business requirements and company objectives. Performs Central Monitoring activities. Evaluates and approves service level agreements. Oversees service providers to perform core data management functions including CRF, edit check development, eCOA, user acceptance testing, data cleaning, reviewing listings, and database locking procedures. Evaluates and makes recommendations related to inter- and intra-departmental processes in order to identify and implement efficiencies and quality improvement measures. How You'll Spend Your Day 1. Leads and manages Data Management tasks outsourced to external vendors and ensures that milestones, deliverables, quality and timelines are met within budget and in accordance with regulatory requirements. 2. Executes according to the Data Management outsourcing and related strategies and processes, developing positive partnerships with CROs and ensuring a high standard of deliverables is maintained. 3. Executes according to the Central Monitoring plan, reviewing Central Monitoring systems for issues, leding/participating in the Central Monitoring risk review meetings. 4. Serves as the Data Management and Centralized Monitoring focal point on assigned studies for all local interfaces and preserves a fluent workflow with the other interfacing departments and local procedures and processes. 5. Supports collaboration, communication, coordination and prioritization within the department working in conjunction with Clinical Programming Lead. 6. Participates and contributes to local and global departmental activities, projects and tasks, in close collaboration with Strategic Planning. 7. Represents Data Management and facilitates project related integration with other groups, notably Clinical Research, Clinical Programming, Statistics, CQA and Regulatory. 8. Collaborate with other Clinical Trial Data Management leads upon need (e.g. Coding). 9. Prepares and maintains timelines and resource plans for the assigned studies, and communicates to management any timeline or resource issues so that appropriate actions can be taken. 10. Attends investigators' meetings; gives input into the presentations that involve relevant data management topics; oversees presentations delivered by service providers or gives presentations. Ensures appropriate training for study team. 11. Approves Data Management Plans for completeness and accuracy of required documentation according to SOP. 12. Provides input into CDMS requirements, assuring protocol requirements are met. Oversees and performs UAT on CDMS components as needed. 13. Acquires knowledge related to drug development, clinical trials methodology, and applies the relevant information in recommending changes in data management to better satisfy business requirements. 14. Follows Teva Safety, Health, and Environmental policies and procedures. 15. Conducts other projects and tasks as assigned.