Associate I, Clinical Pharmacology Scientific Support & Reporting

AbbVie • North Chicago, IL

108d

About The Position

To build all necessary data/information needed to prepare internal documents/scientific reports related to clinical trials by assisting with ongoing blinded efficacy and safety reviews.

Requirements

• Bachelor's degree in Science, related to Field with +2 years' experience in pharmaceutical industry.
• Or Masters degree in pharmacology or related field.
• Associates degree/RN with 6+ years of experience in pharmaceutical industry may be additionally considered.
• Must possess good oral and written communication skills.
• Ability to use computer to generate reports, analyze data, and create presentations.
• Previous experience may be narrowly-focused or limited.
• Ability to identify opportunities and participate in process improvement initiatives.

Responsibilities

• Prepare scientific reports (e.g., Phase 1 Clinical Study Reports and Protocols) and presentations related to clinical trials using available software and templates.
• Comply with procedures set forth in relevant IQS documents and Study protocols.
• Comply with the directives issued by the management regarding clinical studies.
• Commit to producing work of the highest quality.
• Pay close attention to detail.
• Perform literature and competitive intelligence searches.
• Apply experience to analyze clinical study data, using available software to assist with ongoing blinded/un-blinded pharmacokinetic analysis.
• Responsible for receiving and completing assignments and tasks from functional Scientific Staff or Therapeutic Area MD within a given time period with supervision.

Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k) to eligible employees
• Short-term incentive programs

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree