Clinical Pharmacology: Reporting & PK Data Associate I

Allergan; North Chicago (IL); On-site; USD 85,000 - 120,000; Full time

Job summary

AbbVie, based in North Chicago, IL, seeks a scientific professional to prepare reports and presentations for clinical trials, assist with Phase 1 planning and write Phase 1 protocols. The role requires adhering to IQS procedures and management directives while delivering high-quality work with meticulous attention to detail.

Responsibilities include literature searches, competitive intelligence, and applying PK analysis using available software.

Qualifications

• Bachelor’s degree in Science or related field with 2+ years of pharma industry experience.
• Masters degree in pharmacology or related field.
• Strong oral and written communication skills.
• Experience using software to generate reports and analyze data.
• Experience participating in process improvement initiatives.

Responsibilities

• Prepare scientific reports and presentations related to clinical trials using available software and templates.
• Assist in constructing phase 1 clinical study planning documents and write Phase 1 protocols.
• Comply with procedures in IQS documents and Study protocols.
• Comply with directives issued by management regarding clinical studies.
• Commit to producing work of the highest quality and pay close attention to detail.
• Perform literature and competitive intelligence searches.
• Apply experience to analyze clinical study data, using software for PK analysis.
• Receive and complete assignments from Scientific Staff or Therapeutic Area MD within deadlines.

Skills

Communication

Data analysis

Presentation

Process improvement

Education

Bachelor's degree in Science

Masters in pharmacology or related field

Associate degree / RN with 6+ years experience

Job description

AbbVie, based in North Chicago, IL, seeks a scientific professional to prepare reports and presentations for clinical trials, assist with Phase 1 planning and write Phase 1 protocols. The role requires adhering to IQS procedures and management directives while delivering high-quality work with meticulous attention to detail.

Responsibilities include literature searches, competitive intelligence, and applying PK analysis using available software.