Associate Scientist, Clinical I

Employer
AbbVie
Location
Lake County, Illinois, USA
Posted
Mar 08, 2018
Ref
1801753
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.
Qualifications
  • 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