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.
JOB SUMMARY:
The Associate Director, Global Publications will oversee development of strategic publication plans and analyses for multiple therapeutic areas or indications. Ensures globalization of publication plans under their purview resulting in global publication plans. Represents the publications perspective on post-approval teams (PATs) providing therapeutic area (TA) and publications knowledge to guide the teams decisions regarding scientific communications. Interfaces with Medical Affairs and Clinical leadership of assigned TAs to ensure successful integration of publications. Identifies and implements improvements in standards processes to improve efficiencies. Develops and reports metrics to stakeholders with the goal of improving communication and reach of publications. Regularly interfaces with internal stakeholders to determine needs and ensure successful implementation of yearly initiatives. Position can be located in Irvine, California or Madison, New Jersey.
The employee must conduct their work activities in compliance with all AbbVie/Allergan internal requirements and with all applicable regulatory requirements. AbbVie/Allergan internal requirements include compliance with ethics, environmental health and safety, financial, human resources, and general business policies, requirements and objectives.
KEY DUTIES AND RESPONSIBILITIES:
1. Oversee publication strategy development and lead strategic analysis, including providing recommendations regarding publication strategy and effectively integrating strategic concepts from all stakeholders. Ensure strategic objectives are achieved within design of tactical plan. Serve as the functional lead of the publications subteam of the PAT and represent the subteam in PAT meetings as appropriate. Communicate effectively across functional areas and to senior-level management, ensuring that all presentations are tailored to the audience.
2. Ensure successful execution of strategy by overseeing tactical execution of publication plan within established timelines and in adherence to standardized processes. Provide oversight and direction to Global Medical Affairs Publishing staff and external vendors in the development of publication activities for assigned products. Ensure publication projects are reviewed for alignment with strategic objectives. Independently address and resolve situations as they arise or appropriately identify when to elevate to management for resolution. Champion compliance initiatives and ensure compliance documentation is accurate and up-to-date.
3. Provide managerial oversight of direct reports. Determine resource requirements, participate in hiring processes, and ensure successful integration of personnel into the PPTs. Ensure all Performance HR responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention.
4. Maintain current awareness of and serve as an expert resource to PAT and external vendors on good publication practices, editorial policies, and Allergan Publication Policy and standardized processes, and apply to publishing projects. Establish and maintain current awareness of therapeutic area, product knowledge, and competitive landscape in support of publication activities.
5. Actively participate in departmental projects and activities. Ensure publication-tracking documents and data provided for departmental reports are accurate, timely, and audience-appropriate (eg, Quarterly Report). Act as subject matter expert regarding computer-based technologies utilized by the department.
Qualifications
MINIMUM REQUIREMENTS
Desired Experience and Knowledge
* Leadership
* Demonstrated ability to manage and motivate a team without reporting relationship authority
* Demonstrated ability to develop and manage a strong and stable network within the internal organization
* Previous responsibility for managing key vendor relationships
* Demonstrated ability to identify novel strategic initiatives that improve communications
* Scientific communication
* Prior ownership for developing and executing scientific strategic plans and tactics focused on various audiences
* Experience in developing scientific communication strategies and tactics, including the launch of new products and lifecycle management activities for specific audiences (investigators, payers, thought leaders, trade associations, etc.)
* Business Generalist
* Experience in executing and in overseeing highly complex programs and projects
* Strategic planning experience required
* Experience working in a highly matrixed organization
* Working knowledge of the Allergan contracting process
Education and Experience
* Ph.D in a scientific discipline and 6 years publications experience OR MS in a scientific discipline and 9 years publications experience
Essential Skills and Abilities
* Customer Focus: Makes customers and their needs a primary focus of ones actions; develops and sustains productive relationship
* Establishing Strategic Direction: Establishes and commits to a long-range course of action after analyzing information and assumptions; takes into consideration resources, constraints, and organizational values.
* Driving Execution: Translates strategy into operational reality. Breakes down strategic priorities or business initiatives into key tasks and identifies accountabilities. Aligns communication, people, culture, processes, resources and systems to ensure effective implementation and delivery of required results.
* Building Partnerships: Identifies opportunities and takes action to build strategic relationships between ones area and other areas, teams, departments, units, or organizations to help achieve business goals.
* Building Trust: Interacts with others in a way that gives them confidence in ones intentions and those of the organization
* Information Monitoring: Sets up ongoing procedures to collect and review information needed to manage an organization or ongoing activities within it.
* Demonstrated technical abilities and skills in the use and management of the Datavision and other software applications, i.e., Microsoft Outlook, Office, Excel, PowerPoint and Access.
* Ability to exercise good business judgment.
* Strong platform style, ability to make group presentations at regional and national meetings as required.
* Available for limited travel.
Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
Yes, 25 % of the Time
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
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.
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.