Manager, Clinical Data Sciences (CDISC) (On-Site, IL or NJ Based) - 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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. 

Purpose:

Leverage advanced data analysis skills to create innovative approaches to prepare complex data analyses and models that help solve business problems and deliver significant measurable impact. Act as an analytics expert and liaise with cross-functional stakeholders in clinical development to discuss complex data related requirements and opportunities to leverage advanced analytics techniques to drive business value.

Responsibilities:

• Drives the execution of all DSS processes and systems related to the analysis and utilization of data
• Performs analysis tasks in support of clinical trial integrity
• Actively collaborates with DSS stakeholders to provide objective evidence in support of clinical analyses. Ensures consistency across deliverables within and across therapeutic areas and business partners
• Identifies opportunities for process improvement and value creation by using objective data-based evidence
• Identifies opportunities for leveraging advanced analytics techniques and methods to drive business value.
• Develop solutions that bring critical insights to wide scale of different problems
• Develop, prototype and test methods and algorithms on data sets, both small and large. Leverage emerging statistical methodologies to drive innovation in the clinical trial data realm.
• Keep abreast of new and current including technologies and methodologies that can support the utilization of clinical data and DSS operational data to produce efficiencies and create new value propositions.
• Train other team members to support the use of data analytics tools in support of leveraging clinical data and DSS operational data
• Lead a cross-functional data review team in support of clinical trial life cycle; Influences key stakeholders across functions and across hierarchies. Oversee the delivery of data analysis and review deliverables. Ensure alignment across DSS.

*This position will be required to sit on-site 3 days / week*

• Minimum Education: Bachelor’s degree Statistics, Bioinformatics or equivalent field . Master’s degree preferred
• Must have 4+ years of clinical research or analytics related experience (and/or applicable work experience); including 2 years (and/or applicable work experience) demonstrating a high level of core, technical and leadership competencies through cross-functional initiatives.
• Demonstrated intermediate SAS and/or SQL programming skills and expert knowledge of database concepts. Proficiency in R, SAS or other statistical packages
• In-depth knowledge of CDASH and SDTM Standards In-depth understanding of clinical trial processes
• Advanced knowledge of statistical and data mining techniques
• Distinctive communications skills and ability to communicate analytical and technical content in an easy to understand way
• Intellectual curiosity, along with excellent problem-solving and quantitative skills, including the ability to disaggregate issues, identify root causes and recommend solutions
• Demonstration of successful coaching/ mentoring.
• Demonstration of successful execution in a fast-paced environment managing multiple priorities effectively.
• Proven leadership with ability to inspire others and build strong relationships

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

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• 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 short-term incentive programs. ​

• This job is eligible to participate in our long-term incentive programs​

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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. ​

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AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion.  It is AbbVie’s 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.

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