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Cytel

Senior Clinical Data Manager

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Senior level
In-Office or Remote
Hiring Remotely in United States
Senior level

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The Senior Data Manager

The Senior Data Manager brings advanced understanding of the clinical data management process from study start-up through database lock, including database design and data validation as per the requirements in the clinical study protocols, data review plan, & data management plan. The scope of this role may span multiple programs.

Responsibilities

Key responsibilities may include:

 

  • Responsible for end-to-end data management activities and vendor oversight activities across global development programs. 

  • Represents data management function on a client in-house Data Management model for all data related deliverables, especially in support of key decision points and regulatory submissions. 

  • Contributes influential leadership in collaboration with other client Stakeholders to ensure established milestones and deliverables are met with the highest degree of quality.

  • Partners with appropriate stakeholders to mitigate and resolve risks.

  • Provides input to functional governance with client strategic suppliers.  Partners with appropriate stakeholders to resolve issues escalated from the vendor and/or cross-functional teams.

  • Participates in preparing function for submission readiness and may represent function in a formal inspection or audit.

  • Participates and represents function in formal inspections and audits as requested.

  • Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents.

  • Ensures achievement of major data management deliverables and milestones in coordination with other functions including Clinical Operations, Statistical Programming and Statistics.

  • Acts as a process expert for data management operations and team oversight.

  • Maintains SOPs, process maps and templates and timelines to support function’s operational models. 

  • May prepare metrics to support the function’s KPIs.

  • Represents function in external professional initiatives and organizations such as SCDM, CDISC, DIA, etc. to identify industry best practice and increase the visibility of client.

  • Contributes or Leads functional Continuous Improvement initiatives, providing strategic direction and identifying key deliverables that meet timelines, budget, and are in alignment with company, departmental or functional requirements.

  • Ensure compliance with own Learning Curricula, corporate and/or GXP requirements.

  • Works cross-functionally to ensure the quality of the data in each database and on time delivery, as well as quality of other data management deliverables   

  • Performs other duties as assigned.

Qualifications

Educational qualifications:

  • MS or BS in health-related, life sciences area or technology-related field.

Minimum Work Requirements:

  • Minimum of 5 years data management and/or drug development process with expertise in the cross-functional interfaces with the data management function.

  • Proven track record of strong project management skills and experience managing data management activities for large drug development programs.

  • Experience with all phases of development in one or more therapeutic areas preferred.

  • Ability to handle multiple development programs simultaneously.

  • Strong knowledge of data management best practices & technologies as applied to clinical trials.

  • Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes.

  • Expert knowledge of FDA and ICH regulations and industry standards applicable to data capture and data management processes.

  • Advanced knowledge of broad drug development process with expertise in the cross-functional interfaces with the data management function.

Special Skills:

  • Experience in a CRO environment or client in-house data management model.

  • Strong knowledge of relational databases and experience using multiple clinical data management systems.

  • Preferred experience with Medidata RAVE

  • Expert knowledge of general medical terminology, medical coding, laboratory reference ranges, clinical diagnostic procedures, anatomy/physiology and nature of disease processes.

 

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