Aesthetics Clinical Development Lead

AbbVie; California; On-site; USD 120,000 - 180,000; Full time

Job summary

AbbVie is seeking a senior technical writer to prepare scientific reports for clinical trials, using templates and software to ensure accuracy and compliance. You will coordinate advisory meetings, slide decks, and agreements supporting program progress.

The role requires deep understanding of clinical study principles, data analysis, and ability to lead multi-disciplinary teams while delivering high-quality documentation on tight timelines.

Qualifications

• Bachelor’s or Master’s degree in a science field with extensive pharma industry experience, or PharmD/PhD with related expertise.
• Ability to interpret complex clinical study data and generate reports and posters.

Responsibilities

• Prepare scientific reports/presentations for clinical trials using templates and software.
• Coordinate advisory meeting agendas and slide decks.
• Ensure compliance with IQS and study protocol directives.
• Lead study development with electronic document conventions to maintain scientific integrity.
• Collaborate with teams to improve processes and timelines.
• Analyze clinical study data including PK/safety/efficacy reviews.

Skills

Scientific reporting

Study design understanding

Written communication

Project leadership

Education

Bachelors/Master’s in Science

PharmD/PhD

Tools

Statistical analysis software

Templates for clinical reports

Job description

AbbVie is seeking a senior technical writer to prepare scientific reports for clinical trials, using templates and software to ensure accuracy and compliance. You will coordinate advisory meetings, slide decks, and agreements supporting program progress.

The role requires deep understanding of clinical study principles, data analysis, and ability to lead multi-disciplinary teams while delivering high-quality documentation on tight timelines.