Company Description

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 Twitter, Facebook, Instagram, YouTube and LinkedIn.

Job Description

*Position will need to be hybrid (3 days per week onsite) in one of our AbbVie office locations (Lake County, IL, Irvine, CA, Madison, NJ, or South San Francisco, CA)

Purpose:

Lead Publications Teams in the execution of publication plans for assigned assets, and oversee the execution of scientific publications (i.e., clinical manuscripts, abstracts, posters, and oral presentations) that fulfill strategic publication plan and scientific communications objectives for the asset. Ensure Publication Plan is in alignment with the strategic publication plan as developed by the Scientific Communication Platform lead or Medical Affairs plans as applicable.

Responsibilities:

Serve as the leader of cross-functional Publications Team(s) for assigned assets, including leading team meetings/discussions and driving the execution of publication plans, incorporating input from key global stakeholders

• Lead tactical execution of publication plans (i.e., clinical manuscripts, abstracts, posters, and oral presentations), meeting established timelines and budgets
• Review all publications in assigned TA to ensure quality and alignment with Scientific Communication Platforms and supporting communications
• Partner with the Scientific Communications Associate Director to ensure incorporation of scientific platform and medical objectives into publication strategy and tactics
• Partner with Publications Associate Director to project and manage outsourcing budget and internal resource needs for assigned/assets
• Provide managerial oversight to internal and external medical writers regarding assigned projects, ensuring a high-quality and timely work product and adherence to Publication Policy and associated Procedures
• Provide direction to external vendors to effectively complete the execution of publication projects, within specified timelines, and ensure quality publication deliverables
• Address and resolve publications-related issues for assigned therapeutic areas and assets. Ensure project information in publication records and resourcing tools is accurate and up-to-date

Qualifications

List required and preferred qualifications (up to 10). Include education, skills and experience.

• Minimum of Bachelor’s Degree required. PhD, PharmD preferred. Relevant professional certification/credential (e.g., CMPP, AMWA) is a plus.
• 4-5 years of medical/scientific publications (or related) experience required. Pharmaceutical industry or related (e.g., medical communication agency) experience required
• Oncology experience preferred
• Ability to understand and interpret medical data required
• Knowledge of product therapeutic area preferred; working knowledge of statistical concepts and techniques required
• Knowledge of clinical/scientific publication structure, content, and quality required
• Knowledge of scientific publication regulations and best practices required
• Excellent communication skills, both written and verbal, with demonstrated success in creating and delivering effective presentations to senior-level audiences
• Builds strong relationships with peers and cross functionally with partners outside of the team to enable higher performance. Possesses collaborative teamwork and leadership track record
• Ability to form, maintain, and lead productive cross-functional working teams, including addressing issues that arise
• Experience with Datavision preferred

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 posting based 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 or less 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. ​

• This job is eligible to participate in our long-term incentive programs​

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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, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s 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, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because 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, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html