Senior Manager, Clinical Data and Reporting Standards - California, United States - AbbVie

AbbVie California, United States

17 hours ago

Full time

Description

Company Description

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 immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us Follow @abbvie onTwitter,Facebook,Instagram,YouTubeandLinkedIn.
Job Description

The Senior Manager, Clinical Data and Reporting Standards (CDARS) proactively participates in the development of data and reporting standards in support of AbbVies portfolio of clinical trials and ensuring AbbVies conformance to CDISC standards and industry best practices. 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:

Leading or participating in a cross-functional team of subject matter experts to define at least one of the following types of standards within the assigned therapeutic area:

Data Collection

Data Review Rules

SDTM mapping

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.

Support educating the organization on the proper use of standards in pipeline activities by contributing to the development of training materials.

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

Oversee the creation of SDTM , annotated CRF and Clinical Study Data Reviewers 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 AbbVies 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.

May manage 3 or more direct reports. This role can be based remotely anywhere within the U.S.
Qualifications

MS with 9 years of relevant clinical research experience, orBS with 11 years of relevant clinical research experience.

Experience leading development of standards for data collection, tabulation, analysis and/or reporting.

Experience with at least two of the following standards: CDASH, SDTM, ADaM, Analysis Results Metadata, or TLF standards.

Active participation in CDISC teams preferred.

Experience with preparing SDTM and/or ADaM datasets and documentation for regulatory submissions.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture.

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

This job is eligible to participate in our short-term incentiveprograms.

This job is eligible to participate in our long-term incentiveprograms Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employee remains in the Company's sole andabsolutediscretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent withapplicable law. AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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