Associate Clinical Scientist II

Lake County, IL, US
Jan 18, 2019
Required Education
Position Type
Full time
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 Includes:

  • Prepare scientific reports and presentations related to clinical trials using available software and templates.
  • Review clinical protocols and key decisions impacting project timelines with management.
  • 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/ preclinical studies.
  • Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded efficacy and safety reviews and ensure the scientific integrity of all processes.
  • Integrate clinical trial data across studies and identify issues impacting projects and provide this information to internal peers and therapeutic area management.
  • 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.
  • Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
  • Responsible for receiving and completing tasks and assignments from Therapeutic Area MD or Scientific Staff within timeline with minimal supervision
  • Responsible for maximizing individual, therapeutic area and team productivity; and mentor therapeutic area personnel.

  • Bachelors/Master's degree, in Science related to Field with +8 years' experience in pharmaceutical industry
  • Understanding of clinical study principles
  • Must possess good oral and written communication skills
  • Must be proficient in using computer to analyze clinical study data, generate reports and create presentations, posters and manuscripts
  • Must have knowledge of complex scientific analyses, business-related procedures, and project leadership.
  • Experience supporting clinical research, drug development and/or therapeutic area operations.
  • Must have a proven record of successful projects.
  • Ability to produce work of the highest quality by paying attention to detail
  • Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
  • Independent expertise/experience to analyze clinical study/statistical data by using available software.

Equal Opportunity Employer Minorities/Women/Veterans/Disabled