Manager - Data Standards, SDTM Programming (Hybrid)

BioSpace; Irvine (CA); On-site; USD 140,000 - 190,000; Full time

Benefits offered by this job

PTO & Holidays

Medical/Dental/Vision Insurance

401(k) & Benefits

Long-term Incentive Programs

Job summary

AbbVie is seeking a Manager, Clinical Data and Reporting Standards (CDARS) to drive governance and deployment of data standards across AbbVie's clinical trials. You will lead SDTM/ADaM mappings, data collection rules, and study-level tables while ensuring conformance to CDISC standards and regulatory expectations.

The role requires cross-functional collaboration, development of training materials, and ongoing communication of standards initiatives to the organization.

Qualifications

• Experience leading development of data standards for collection, tabulation, analysis and reporting.
• Experience preparing SDTM/ADaM datasets and documentation for regulatory submissions.
• Strong collaboration with cross-functional teams to align standards across SDTM, ADaM and CDASH.

Responsibilities

• Participate in cross-functional teams to define data standards within therapeutic areas (e.g., data collection, data review rules, SDTM/ADaM mappings).
• Oversee SDTM datasets, define.xml, annotated CRFs, and study data reviewers guides for regulatory submissions (FDA/PMDA).
• Provide guidance on conformance issues for SDTM/ADaM and resolve data/metadata issues with study teams.

Skills

SDTM programming

CDISC standards

Data governance

Education

MS in clinical research

BS in clinical research

Job description

< h3>Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

The Manager, Clinical Data and Reporting Standards (CDARS) proactively participates in the development of data and reporting standards in support of AbbVie's portfolio of clinical trials and ensuring AbbVie's conformance to CDISC standards and industry best practices as well as pipeline based SDTM development. This role implements the strategy and framework for governance of standards as set by the Head and Associate Directors of CDARS and actively engages in deployment of next generation process and technology.

Standards Development responsibilities include

Actively participating with a cross-functional team of subject matter experts to define one more of the following types of standards within the assigned therapeutic areas:

• Data Collection
• Data Review Rules
• SDTM mapping
• Participating in a cross-functional team of subject matter experts to define one more of the following types of standards within the assigned therapeutic areas:ADaM mapping and derivation
• Study-level tables, listings, or figures
• Product-level safety analysis displays

Ensuring each standard is clearly defined, with appropriate documentation of relevant assumptions and decisions related to its use to support pipeline activities

Ensuring consistency across standard types (e.g. eCRF standards align with TLF standards, SDTM standards align with ADaM standards, etc.)

Develop training materials to the organization on the proper use of standards in pipeline activities

Communicate ongoing standard development activities across the organization

Pipeline responsibilities include

• Providing feedback on CRF design and SDTM datasets to ensure data are collected and represented in a manner that support regulatory requirements to comply with CDISC standards (CDASH, SDTM and ADaM) and AbbVie standard extensions to CDISC
• Review and provide feedback on SDTM Trial Design Domains
• SDTM Programming based on SDTM specifications
• Oversee the creation of SDTM datasets, define.xml, annotated CRF and Clinical Study Data Reviewer’s Guides for both FDA and PMDA submissions
• Consult on conformance issues for SDTM and/or ADaM and work with the study team to resolve the problem either by correcting the data or metadata, or by providing an appropriate explanation

Other Responsibilities Include

• representing AbbVie’s interests in industry standards development projects,
• staying current with industry standards such as CDISC, and the regulatory requirements related to their use
• identifying improvements to the processes and content of standards, and driving those improvements to completion

Qualifications

Minimum Qualifications

• MS with 8 years of relevant clinical research experience, or
• BS with 10 years of relevant clinical research experience

Experience With SDTM Programming 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

Preferred Experience

• Experience with CDASH is highly recommended
• Experience with ADaM, Analysis Results Metadata, or TLF standards are 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.

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.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html