Clinical Pharmacology Associate: Reporting & Study Support

AbbVie; North Chicago (IL); On-site; USD 70,000 - 100,000; Full time

Job summary

AbbVie in North Chicago seeks a scientifically trained professional to prepare reports and presentations for clinical trials, assist Phase 1 study planning, and ensure strict adherence to study protocols and IQS documents.

You will perform literature searches, analyze pharmacokinetic data, and support assignment completion under supervision, contributing to high-quality outcomes in a fast-paced environment.

Qualifications

• Bachelor’s degree in Science or related field; +2 years pharma experience or Master’s in pharmacology
• Associates degree/RN with 6+ years pharma experience may be considered
• Strong written and oral communication skills
• Computer skills to generate reports, analyze data, and create presentations
• Experience may be narrow; identify opportunities and contribute to process improvements

Responsibilities

• Prepare scientific reports and presentations for clinical trials using templates
• Assist in constructing Phase 1 study planning documents and write Phase 1 protocols
• Ensure compliance with IQS documents and study protocols
• Follow directives from management regarding clinical studies
• Deliver high-quality work with attention to detail
• Perform literature and competitive intelligence searches
• Analyze clinical study data using available software for PK analyses
• Handle assignments from Scientific Staff or Therapeutic Area MD within set timelines

Skills

Communication skills

Attention to detail

Data analysis

Literature review

Education

Bachelor’s degree in Science-related field

Master's in pharmacology or related field

Associates degree or RN with 6+ years in pharma

Tools

Excel

Reports/Presentation tools

Statistical software

Job description

AbbVie in North Chicago seeks a scientifically trained professional to prepare reports and presentations for clinical trials, assist Phase 1 study planning, and ensure strict adherence to study protocols and IQS documents.

You will perform literature searches, analyze pharmacokinetic data, and support assignment completion under supervision, contributing to high-quality outcomes in a fast-paced environment.