Clinical Pharmacology Scientific Support Associate

2 weeks ago

Chicago, Illinois, United States AbbVie Full time
Job Overview

AbbVie is seeking a highly skilled Clinical Pharmacology Scientific Support Associate to join our team. As a key member of our scientific support team, you will play a critical role in building all necessary data and information needed to prepare internal documents and reports related to clinical trials.

Key Responsibilities:

  • Prepare scientific reports and presentations related to clinical trials using available software and templates.
  • Responsible for writing basic protocols and clinical study reports.
  • Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical studies.
  • 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.
  • Responsible for receiving and completing tasks and assignments from function or Therapeutic Area MD or Scientific Staff within timeline with minimal supervision.
  • Perform literature and competitive intelligence searches.
  • 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.
  • Appropriate and effective use of resources to complete tasks and meet required timelines.
  • Responsible for maximizing individual, function/therapeutic area and team productivity; and mentor function/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 function/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.

Additional Information:

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

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