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Senior Director, Scientific

Senior Director, Scientific

BioSpaceChicago, IL, US
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Overview

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 X, Facebook, Instagram, YouTube, LinkedIn and TikTok.

Job Description

The Sr. Director has responsibility and accountability for Epidemiology strategic research plans and agendas, execution of studies and projects within those plans for a portfolio of assets / brands / indications across a therapeutic area and leads a team of scientists with global reach. Guides and counsels across TA worldwide management and senior leadership of epidemiology's role in generating impactful evidence across the multiple indications of the relevant TAs. Able to influence the enterprise level, effectively manage and prioritize resources and develop and retain a high performing team. Reporting to the VP, Head of Epidemiology, the Sr. Director is a member of Global Epidemiology LT and is expected to influence and shape team culture and capabilities.

Responsibilities

  • Highly effectively communicates findings to internal leadership (Executive Leadership, Area VPs, GMs etc.) and external (e.g. Regulatory Authorities, KOLs etc.).
  • Accountable for the creation of strategic plans for all products within the TAs for which the role has oversight and to ensure strategic plans within the TAs remain relevant to product development and the marketplace.
  • Leads interactions with cross-functional leaders for that TA and directs the design, conduct, and analysis of projects within each product area strategy across multiple programs.
  • Drive the design and execution of a high-quality Epidemiology program supporting the therapeutic area strategy for pipeline products and on-market products that meet ethical, scientific, regulatory, commercial, and quality requirements.
  • In the post-marketing setting, responsible for developing and executing post-marketing commitments and requirements as well as other safety and effectiveness evidence.
  • End-to-end delivery of Global Epidemiology book of work under their remit, from strategy development to content pull through.
  • Ensure strong partnership with all relevant Clinical Science functions and Global Epidemiology CoEs to ensure a comprehensive voice in cross-functional meetings.

Qualifications

  • Advanced degree (MD, PharmD, PhD / MS) in (pharmaco)epidemiology.
  • Minimum of twelve years working experience with a Masters, ten years with PhD (fellowship experience acceptable).
  • Typically 10+ years of clinical development experience in the pharmaceutical industry, CRO, academia or health-related consulting; expert knowledge in a relevant therapeutic specialty. Clinical research experience strongly recommended; within pharmaceutical industry preferred.
  • Ability to navigate uncharted territory with few established guidelines; capable of directing compliance knowledgeably and expeditiously.
  • Ability to develop creative and effective solutions to resource constraints and cross-program priorities; experience leading complex products and / or clinical development in support of pipeline development and on-market product support preferred.
  • Extensive knowledge of the global regulatory landscape and related development functions across all phases of drug development.
  • Skills to lead a cross-functional team and manage scientific personnel in clinical research; self-starter with a drive to achieve commercial success.
  • High goal-orientation with the ability to solve problems as projects encounter ups and downs in drug development or on-market support.
  • Proven people leadership and ability to lead leaders; enterprise strategic influencer.
  • Additional Information

  • The compensation range described below is the range of possible base pay compensation the Company believes in good faith it will pay for this role at posting time, based on job grade. Individual compensation will depend on location and may be higher or lower than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off, medical / dental / vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term and long-term incentive programs.
  • Note : No amount of pay is considered wages or compensation until earned, vested, and determinable; compensation and benefits are at the Company’s discretion subject to applicable law.
  • AbbVie is an equal opportunity employer and is committed to integrity, innovation, and serving our community. EEO / Veterans / Disabled.
  • US & Puerto Rico only - equal employment opportunity information : https : / / www.abbvie.com / join-us / equal-employment-opportunity-employer.html

    US & Puerto Rico applicants seeking a reasonable accommodation : https : / / www.abbvie.com / join-us / reasonable-accommodations.html

    Seniority level

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