AbbVie Senior Associate, Clinical Scientist I in Lake County, Illinois

To build all necessary data/information needed in preparing internal documents/scientific reports related to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking.

Key Responsibilities Include: * Prepare scientific reports/presentations related to clinical trials using available software and templates and; review/contribute to clinical protocols, by utilizing expertise, to assist in interpretation of data. * Coordinate advisory meeting agendas, activities and slide decks and consulting agreements. * Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical studies. * Lead the study development by applying most current electronic document conventions/processes most consistently/accurately to ensure scientific integrity of all processes. * Responsible for receiving and completing tasks and assignments from function, Therapeutic Area MD or Scientific Staff within timeline with minimal supervision and; maximizing individual, function/therapeutic area and team productivity. * Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management. * Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded/un-blinded PK, safety and efficacy reviews and ensure the 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 function/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.

Basic: * 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.

Job Classification: Experienced
Primary Location: USA-Illinois-Lake County
Organization: Research & Development
Schedule: Full-time
Shift: Day
Travel: Yes, 10 % of the Time
Req ID: 1706802

Equal Opportunity Employer Minorities/Women/Veterans/Disabled