Job Details

Job Opportunity At AbbVie

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.

To build all necessary data/information needed in preparing internal documents/scientific reports related to clinical studies and research activities for aesthetic clinical development programs. Participates in cross-functional teams to keep multiple deliverables moving forward supporting overall botulinum toxin and aesthetic franchise scientific and business strategy.

Responsibilities:

• Prepare scientific reports/presentations related to aesthetic clinical studies using available software and templates. Review/contribute to clinical protocols, assist in data interpretation.
• Coordinate advisory meeting agendas, activities, slide decks, and consulting agreements.
• Comply with procedures set forth in relevant operational quality documents, investigative protocols with all accompanying regulatory documentation, and other directives issued by the management regarding clinical studies.
• Lead study development by applying current electronic document conventions/processes most consistently/accurately to ensure scientific integrity of all processes.
• Receive and complete tasks/assignments from Therapeutic Area MD/SD and Clinical Development leadership with minimal supervision, maximizing individual contribution for Therapeutic Area and clinical study team productivity.
• Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
• Review clinical study data quality and analyze results, including statistical data using available software, to assist with ongoing blinded/un-blinded safety and efficacy reviews, ensuring scientific integrity of all processes.
• Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
• Provide/present key clinical study information to Therapeutic Area and management.
• May lead teams within Therapeutic Area and supervise exempt and/or non-exempt direct reports and mentor function/-therapeutic area personnel.

Qualifications:

• Bachelors/Master's degree in Science related to Field with 11+ years' experience in the pharmaceutical industry or Pharm-D/PhD with 1+years.
• Ability to understand more complex clinical study principles.
• Advanced understanding of appropriate technology necessary to analyze clinical study data, generate reports and create presentations, posters, and manuscripts.
• Experience in team, drug development, and scientific project leadership or related.
• Experience supporting clinical research, drug development, and/or function/Therapeutic Area operations.
• Must have a proven record of successful projects.
• Experience in multi-faceted, broad-based multiple functions/therapeutic areas or clinical functions with in depth knowledge of clinical study issues.
• Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
• Ability to produce work of the highest quality by paying attention to detail.
• Must possess good oral and written communication skills.

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

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.