Jobs · Legal · Illinois

Senior Manager, Value Writer

AbbVie · Mettawa, IL · 1 wk ago
LegalFull-time

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 including immunology, oncology and neuroscience—and products and services in our Allergan Aesthetics portfolio.

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 (e.g., clinical manuscripts, abstracts, posters, and oral presentations), meeting established timelines and budgets
  • Review all publications in assigned therapeutic area to ensure quality and alignment with Scientific Communication Platforms and supporting communications
  • Partner with the Scientific Communications Director to ensure seamless transfer of the scientific publications strategic plan and oversee pull-through to publication plan and supporting tactics
  • Partner with Publications 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
  • Ensure all performance assessment responsibilities are achieved for direct reports. Provide training and feedback, resolve personnel issues, and manage talent retention for assigned staff
  • 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

  • Minimum of Bachelor’s Degree required. PhD, PharmD, or Master’s Degree 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
  • Demonstrated abilities in a leadership capacity required
  • 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. Knowledge of scientific publication regulations and best practices
  • 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. Collaborative teamwork and leadership track record
  • Ability to form, maintain, and lead productive cross-functional working teams, including addressing issues that arise
  • Microsoft Office and Internet navigation proficiencies essential

Benefits

  • Comprehensive package of benefits including paid time off (vacation, holidays, sick)
  • Medical, dental, and vision insurance
  • 401(k) eligibility
  • Eligibility to participate in long-term incentive programs

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