Manager, Clinical Data and Reporting Standards - SDTM Programming (Hybrid)

About the role

The Manager, Clinical Data and Reporting Standards (CDARS) plays a crucial role in developing and implementing data and reporting standards for AbbVie's clinical trials. This individual ensures compliance with CDISC standards and industry best practices, and drives the development of next-generation processes and technologies.

Responsibilities

• Actively participates in defining standards within assigned therapeutic areas, including Data Collection, Data Review Rules, SDTM mapping, ADaM mapping, and study-level tables, listings, or figures.
• Ensures consistency across standard types and develops training materials for proper use of standards in pipeline activities.
• Provides feedback on CRF design and SDTM datasets to ensure compliance with CDISC standards and AbbVie extensions.
• Reviews and provides feedback on SDTM Trial Design Domains and SDTM Programming based on specifications.
• Oversees the creation of SDTM datasets, defines.xml, annotated CRFs, and Clinical Study Data Reviewer’s Guides for both FDA and PMDA submissions.
• Consults on conformance issues for SDTM and/or ADaM and works with the study team to resolve problems.
• Represents AbbVie’s interests in industry standards development projects and stays current with regulatory requirements.
• Identifies and drives improvements to processes and content of standards.

Qualifications

• MS with 8 years of relevant clinical research experience, or BS with 10 years of relevant clinical research experience.
• Experience with SDTM is required.
• Experience leading development of standards for data collection, tabulation, analysis, and/or reporting.
• Experience with preparing SDTM and/or ADaM datasets and documentation for regulatory submissions.
• Experience with CDASH is highly recommended.
• Experience with ADaM, Analysis Results Metadata, or TLF standards is helpful.
• Active participation in CDISC teams preferred.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and 401(k) to eligible employees. This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, and serving our community. Equal Opportunity Employer/Veterans/Disabled.