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 atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

Job Description

Purpose:
Central Monitoring and Risk Management is at the heart of AbbVies end-to-end RBQM modela critical pillar
required in AbbVies mission to be a world-class R&D organization.
The purpose of the Sr. Central Monitor is to analyze & investigate study data utilizing Key Risk Indicators, Quality Tolerance Limits and Data Anomalies at the macro-level for insights that are not visible when monitoring individual data points and study sites. Observations, signals, and data presentations are provided to the primary site monitor or study team members as early as possible, to allow for interventions to mitigate potential risks to participant safety and data integrity.
In addition, the Senior Central Monitor performs integrated data review of subject clinical trial data using a
clinical data review platform. Study specific data checks, as outlined in the integrated data review plan data
listings, are programmed to provide ease of review.
The Senior Central Monitor works closely with cross-functional colleagues (i.e., primary site monitor, safety,
data sciences, and clinical study leadership) to ensure that they understand the data insight and the root
cause, to determine the appropriate actions to mitigate the risk and/or address the issue.
The Senior Central Monitor is AbbVies first responder in identifying, triaging, and escalating studylevel risks.
The Senior Central Monitor function includes team members from across the globe. The Senior Central Monitorwill support more complex assignments, an increased trial workload, support and lead initiatives, and
participate in peer mentoring. Central Monitors are responsible for multiple studies across many therapeutic
areas.

Responsibilities:

• Review the protocol and ensure the Integrated Data Review Plan is updated for the central monitorrole within the study, ensuring key critical data is included in the plan aligned to the role of centralmonitor.

• Provide recommendations during initial Risk Management meetings on appropriate TA or studyspecific Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs).

• Inspect aggregate clinical and operational data from multiple sources (eCRF, vendor data, digitalhealth/wearables, etc.). Utilize data analytics and visualizations to uncover insights and see complexpatterns within data to perform review.

• Use Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Data Anomalies to identifysignificant issues and emerging risks at the study site, program, and country level.

• Document detected issues and emerging risks.

• Translate the issues and emerging risks by clearly outlining the situation, the significance orimplications of data insight, and any further action required.

• Communicate findings as per planned process to ensure that all cross-functional stakeholders havethe same understanding of the issues and emerging risks so that the appropriate follow-up actioncan be taken.

• Provide the primary site monitor with relevant information; allowing monitors to work with site staff and havemore productive discussions with our Investigator partners.

• Work collaboratively in the pursuit of quality with the primary site monitor, the Study Team, and crossfunctional departments.

• Participate in Health of Study and Risk Management Meetings.

• Contribute to the ongoing development, advancement, and improvement of the RBQM systemsproviding requirements that will further enable data analysis (i.e. what to look for, how to best presentthe data so that you can see what youre looking forward) and testing the system at the study levelto ensure system quality

• Assigned to challenging spaces where the criticality of delivery requires proactive planning forexecution on deliverables, seamless responsiveness to work volume increases, and complextherapeutic areas.

• Be a RBQM champion across AbbVie, supporting the execution of RBQM processes as part of crossfunctional teams spanning the R&D portfolio (all therapeutic areas and phases of development).
  

Qualifications

Qualifications:

• Bachelors degree in related fields including life sciences and risk-based disciplines.

• Minimum of 5 years of clinically related or data trend analysis experience; at least 4 years ofclinical research monitoring.

• Experience working in a RBQM model or similar experience with risk-based environment preferred.

• Demonstrated current in-depth knowledge and understanding or willingness to learn of appropriate therapeutic indications, regulations, and ICH/GCP guidelines as they relate to the conduct of clinical trials (studymanagement, data management and regulatory operations). TA experience is preferred in one of the followingareas (Neuroscience, Oncology, Immunology, Eye Care, and Aesthetics.

Additional Information

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, visithttps://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