Senior Clinical Data Manager

Jazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit and follow @JazzPharma on Twitter. The Senior Clinical Data Manager will be responsible for performing Data Management activities that support Jazz Pharmaceuticals'' commercial and development projects worldwide. He/she will participate as an active member of a multi-disciplinary team to plan, lead and execute the Data Management tasks required for phase 1-4 studies. The Senior Clinical Data Manager has a broad, fundamental knowledge of the data management process and is able to perform most required tasks with minimal guidance.The Senior Clinical Data Manager will:Be able to lead a large clinical study or a series of related studies with minimal guidanceRepresents Data Management on the CTWG for assigned studiesProvide mentoring and training to lower level Data Management staff assigned to his/her studiesManage and monitor the progress of data management activities with CROs or other vendors on assigned studies; build effective relationships with CRO / vendor counterpartsReview protocols for appropriate data capture including electronic Case Report Form (eCRF) design.Be able to perform a thoroughly detailed review of eCRF data teract with CRAs, programmers, study managers and statisticians in designing eCRFs and creating the annotated eCRF and CRF completion guidelines.Lead the development of data edit check specifications and data listingsCoordinate the design and testing of Electronic Data Capture (EDC) systems according to company standards. Able to resolve EDC system issues with team membersDevelop or lead the development of the Data Management Plan for a clinical study.Able to review and provide feedback to the clinical team on other study documents e.g. Clinical Monitoring plans, Statistical analysis plans and vendor specificationsMay provide training on the EDC system and/or eCRF Completion Guidelines at Investigator Meetings and to internal and external study team members as neededPerform reconciliation of header data from external data sources against the clinical databasePerform Serious Adverse Event reconciliation activities according to SOPs and guidelinesLead database upgrades/migrations including performing User Acceptance TestingBe able to maintain study workbooks and data management filesPerform database lock and freeze activities per company SOPsParticipate in regular team meetings and provide input when appropriateProvide input into the development of data management SOPs, Work Instructions, and process documents; take a leadership role in the development of assigned documentsContribute to a professional working environment including the application of Jazz Pharmaceuticals Code of Business Conduct and EthicsAssist with the training of new employees and/or contractorsESSENTIAL REQUIREMENTS:Bachelor''s Degree required (Master''s Degree preferred) in the scientific/healthcare field.At least five years'' experience in Data Management for the pharmaceutical/biotechnology industry, or equivalent experience in an FDA-regulated environment, including study lead experienceHas good project management skills and a proven ability to multitaskUnderstands the scope and focus of Phase 1-4 clinical studies, and has a proven ability to perform most of the core Data Management tasks and interact with vendors.Possesses a comprehensive understanding of regulatory guidelines and industry standards (e.g., ICH/FDA guidances, CDISC standards, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries, etc.) and their application to Data Management practice.Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.Possesses strong English language written and verbal communication skills.Experience and understanding of the Oncology or CNS therapeutic area, and with Phase III pivotal studies are preferred.Able to travel to off-site meetings or training seminars as needed.Possesses solid computer system and technical skills with a strong ability to learn multiple computer applications. Prior experience with different Data Management systems and technologies, and Electronic Data Capture systems is desirable.Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.

Created: 2021-11-29