Associate Scientist, Clinical I

Lake County, Illinois, USA
Mar 08, 2018
Required Education
Associate Degree
Position Type
Full time
To build all necessary data and information needed to prepare internal documents/scientific reports related to clinical trials and keep multiple reports moving forward simultaneously through multi-tasking. Key Responsibilities Include
  • Prepare scientific reports and presentations related to clinical trials using available software and templates.
  • Reviews clinical protocols and coordinate advisory meeting agendas, activities, 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.
  • Ensure scientific integrity of all processes by applying current electronic document conventions and processes consistently and accurately.
  • Integrate clinical trial data across studies, identify issues impacting projects and provide the relevant information to internal peers and therapeutic area management.
  • Perform literature and competitive intelligence searches
  • Responsible for receiving and completing tasks and assignments from Therapeutic Area MD or Scientific Staff within timeline with minimal supervision
  • Appropriate and effective use of resources to complete tasks and meet required timelines.
  • Responsible for maximizing individual, therapeutic area and team productivity; and mentor therapeutic area personnel.
  • Bachelors/Master's degree, in Science related to Field, with +5 years' experience in pharmaceutical industry
  • Associates degree/RN with 9+ years of experience in pharmaceutical industry may be additionally considered
  • Understanding of basic clinical study principles
  • Must possess good oral and written communication skills
  • Proficient in using computer to analyze clinical study data, generate reports and create presentations
  • Experience supporting clinical research, drug development and/or therapeutic area operations.
  • Must have proven record of successful projects.
  • Must be able to produce work of highest quality by paying attention to detail
  • Ability to identify opportunities and participate in process improvement initiatives.

Equal Opportunity Employer Minorities/Women/Veterans/Disabled