TA Director, Risk Management Lead Multiple Therapeutic Areas (Hybrid)

AbbVie

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profile Job Location:

North Chicago, IL - USA

profile Monthly Salary: Not Disclosed
Posted on: 13 hours ago
Vacancies: 1 Vacancy

Job Summary

The TA Director of Risk Management Leads is responsible for overseeing and advancing risk management strategy practices and performance across clinical development portfolios within Immunology Neuroscience Aesthetics /Eye Care /Specialty therapeutic areas. This leader drives risk identification assessment mitigation and monitoring ensuring a critical-to-quality data-driven approach is embedded in protocol design and study operations. By developing and leading a high-performing team of Risk Management Leads the TA Director ensures effective oversight RAMP accountability and continuous improvement in risk management practices with a specific focus on addressing resource gaps related to RAMP entry work and the implementation of risk-based study modifications.

Key Responsibilities:

  • Drive portfolio-level risk identification and mitigation strategies in partnership with therapeutic area teams enhancing proactive management of study and program risks.
  • Support and collaborate with the Integrated Evidence Strategy Team (IEST) to embed critical-to-quality elements into protocol design ensuring data collection is focused on decision-making needs.
  • Lead develop and mentor a team of Risk Management Leads fostering expertise collaboration and innovation in risk-based quality management.
  • Oversee the development and execution of therapeutic area risk insights dashboards and mitigation plans promoting a deep understanding of risk drivers and solutions.
  • Ensure robust RAMP (Risk Assessment and Mitigation Plan) processes tracking accountability and ensuring timely data-driven risk action planning.
  • Address resource gaps by overseeing RAMP entry work and supporting the implementation of risk-based modifications to the scope of studies assigned to Study Risk Leads (SRLs) advocating for full resource needs where required.
  • Collaborate with cross-functional stakeholders (including Clinical Site Management Clinical Study Leadership Data Science and Compliance) to ensure alignment and consistency in risk management practices.
  • Contribute to the development standardization and continuous improvement of risk management best practices metrics and training across the organization.

Impact and Influence:

  • Deepens portfolio and program risk management capabilities and accountability.
  • Leads a critical-to-quality focused approach to data collection supporting pipeline decision-making on sound data.
  • Supports a culture of continuous improvement transparency and evidence-driven risk mitigation.

**This is a hybrid position working on-site T-TH.  Candidates must be local to Lake County IL or Irvine CA and work on-site 3 days a week. 

 


Qualifications :

  • Minimum of a bachelors degree in life sciences healthcare pharmacy nursing or a related field; an advanced degree (Masters PharmD PhD MD) is strongly preferred.
  • At least 15 years of experience in clinical research clinical operations or study/data risk management with a minimum of 5 years in a leadership or people management capacity.
  • Demonstrated expertise in risk-based quality management (RBQM) including experience applying ICH-GCP E6(R2) risk-based methodology and risk management best practices in clinical development.
  • Direct hands-on experience with portfolio-level risk assessments Risk Assessment and Mitigation Planning (RAMP) and implementing risk-based modifications across multiple clinical programs/therapeutic areas.
  • Strong knowledge of relevant regulatory guidelines (FDA EMA ICH) Good Clinical Practice (GCP) and global health authority requirements for clinical trials.
  • Professional risk management certifications are highly desirable (e.g. ASQ Certified Manager of Quality & Organizational Excellence Chartered Enterprise Risk Analyst (CERA) Certified Risk Manager (CRM) Professional Risk Manager (PRM) ASQ Risk Management Specialized Credential or equivalent experience).
  • Experience with critical-to-quality (CtQ) elements protocol design input and collaboration with evidence strategy teams preferred.
  • Demonstrated success developing mentoring and leading teams preferably in a matrixed global environment.
  • Advanced skills in data analytics dashboarding and the use of data visualization tools (e.g. Excel Power BI Tableau) for risk oversight and decision-making support.
  • Excellent interpersonal skills; able to communicate complex concepts clearly persuade stakeholders and foster cross-functional collaboration.

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 postingbased 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 orless 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. 

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 commissionincentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paidand may be modified at the Companys 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. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No


Employment Type :

Full-time

The TA Director of Risk Management Leads is responsible for overseeing and advancing risk management strategy practices and performance across clinical development portfolios within Immunology Neuroscience Aesthetics /Eye Care /Specialty therapeutic areas. This leader drives risk identification asse...
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About Company

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AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

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