AbbVie

Associate Director, Precision Medicine Program Management Office

Posted on: 4 Mar 2021

Chicago, IL

Job Description

About AbbVie
AbbVies mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, womens health and gastroenterology, in addition to products and services across its 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 :

The Precision Medicine Program Management Office (PMed PMO) focuses on driving performance through strategic and operational leadership. The PMed PMO serves as a strategic partner for the PMed Leadership Team and is the primary operational contact enabling effective communication and alignment within the PMed organization as well as across relevant functions (PPM, Discovery, Development, etc.). This role is accountable for managing complex initiatives and projects within the PMed organization to ensure appropriate prioritization and resourcing. Works with the PMed Leadership Team to develop project objectives, strategies, timelines, and milestones to advance the pipeline.

Responsibilities :

* Independently drives and influences day to day activities and, with oversight, strategic deliverables to the PMed team ensuring they are efficient and effective across functional boundaries.
* Supports all operational aspects of Precision Medicine Review Forum (PMRF) including aligning scheduling and agendas with existing governance milestones. Serves as a meeting manager.
* Partners with PMed and CDx teams to drive overall program management and ensures timely execution of PMed deliverables across the evolving pipeline.
* Orchestrates overall PMed program implementation across initiatives.
* Tracks initiative progress and results, and ensures timely and coordinated execution of milestones through regular touchpoints with initiative leads (meetings, materials share, etc). Mobilizes and engages with initiatives leads as optimal.
* Ensures regular pulse checks to monitor short-, medium-, and long-term success for PMed program. Proposes and coordinates interventions in response to pulse check results to ensure success.
* Manages interfaces with organization by coordinating communications and change management for key PMed changes, collecting and implementing feedback from key stakeholders.
* Identifies interdependencies and resolves issues across PMED program initiatives. Escalates when necessary.
* Coordinates various program updates (e.g., updates to PMed Team Leaders Forum, DLT, RDLT) and maintains key materials (communication packages, Pre-FIH and CDx guidebooks and workplans, etc.).
* Drives strategic planning and execution across the PMed organization ensuring appropriate prioritization and interdependencies. Ensures PMed program activities are actively tracked and reported across all PMed functions, highlighting potential delays, risks, and developing mitigation plans.

Qualifications
Qualifications:

* 7+ years of experience in the pharmaceutical industry in a variety of roles in at least one role/functional area associated with drug development (research and development, commercial, project management, operations).
* 4+ years in a cross-functional project / program management role.
* Strong program management skills and knowledge of program management practices in the
* pharmaceutical industry and common tools utilized.
* Strong verbal and written communication skills.
* Demonstrated ability to lead without direct authority, ability to excel in a matrixed environment and independently drive to deliver on business objectives.
* Proven track record of developing and executing change management strategies as well as successful project planning and management of highly complex business and technology initiatives.
* Ability to think strategically and cross-functionally across TA program to identify opportunities and make connections to advance business deliverables.
* Applied knowledge of program management tools and processes (e.g., management of integration, scope, time, cost, quality, human resources, communications, risk and procurement).
* Consistently communicates to an executive level in an accurate, regular, concise, and inclusive manner.
* Extensive experience with performance measurement and communication (e.g., metrics, dashboards).

Key Stakeholders :

R&D; and Precision Medicine leadership, Portfolio Program Management, functional and/or area leads.

Significant Work Activities
N/A
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
M
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis 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, protected veteran status, or any other legally protected characteristic.

AbbVie

Chicago, IL

AbbVie Inc. discovers, develops, manufactures, and sells pharmaceutical products in the United States, Japan, Germany, Canada, Italy, Spain, the Netherlands, the United Kingdom, Brazil, and internationally. The company offers HUMIRA, a therapy administered as an injection for autoimmune and intestinal Behçet's diseases; IMBRUVICA to treat adult patients with chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), mantle cell lymphoma, waldenström’s macroglobulinemia, marginal zone lymphoma, and chronic graft versus host disease; VENCLEXTA, a BCL-2 inhibitor used to treat adults with CLL or SLL; VIEKIRA PAK, an interferon-free therapy to treat adults with genotype 1 chronic hepatitis C virus (HCV); TECHNIVIE to treat adults with genotype 4 HCV infection; and MAVYRET to treat patients with chronic HCV genotype 1-6 infection.

It also provides KALETRA, an anti-human immunodeficiency virus (HIV)-1 medicine used with other anti-HIV-1 medications to maintain viral suppression in HIV-1 patients; NORVIR, a protease inhibitor indicated in combination with other antiretroviral agents to treat HIV-1; and SYNAGIS to prevent respiratory syncytial virus infection at-risk infants. In addition, the company offers AndroGel, a testosterone replacement therapy for males; CREON, a pancreatic enzyme therapy for exocrine pancreatic insufficiency; Synthroid to treat hypothyroidism; and Lupron to treat prostate cancer, endometriosis, and central precocious puberty, as well as anemia.

Further, it provides Duopa and Duodopa, a levodopa-carbidopa intestinal gel to treat Parkinson’s disease; Sevoflurane, an anesthesia product; and ORILISSA, a non-peptide small molecule gonadotropin-releasing hormone antagonist for women with moderate to severe endometriosis pain. It has collaborations with Alector, Inc.; Janssen Biotech, Inc.; Galapagos; Bristol-Myers Squibb Company; and Calico Life Sciences LLC. The company was incorporated in 2012 and is headquartered in North Chicago, Illinois.

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