Aesthetics Clinical Development Lead

AbbVie; Irvine (CA); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie in Irvine, CA, is seeking a seasoned clinical trials professional to prepare scientific reports and manage data for multiple ongoing studies. The role focuses on drafting presentations, aligning protocols, and ensuring scientific integrity across studies.

You will coordinate advisory meetings, supervise project work, analyze PK, safety and efficacy data, and contribute to protocol development. A strong background in pharma clinical research and leadership is required, with hands-on

Qualifications

• Bachelors/Master’s degree in science with 11+ years in pharma, or Pharm-D/PhD with 1+ years
• Ability to understand complex clinical study principles
• Advanced tech to analyze data, generate reports, create posters/manuscripts
• Experience leading drug development and scientific projects
• Experience supporting clinical research and therapeutic-area operations
• Proven track record of successful projects

Responsibilities

• Prepare scientific reports/presentations for clinical trials using templates and software
• Coordinate advisory meeting agendas, activities and slide decks
• Comply with IQS, study protocols and directives from management
• Lead study development with current electronic document conventions/processes
• Receive/complete tasks within timelines with minimal supervision
• Participate in process-improvement teams and review key timelines
• Analyze clinical study data including PK, safety, efficacy reviews
• Perform literature/competitive intelligence searches
• Present key study information to management
• May lead teams and mentor personnel

Skills

Clinical study leadership

Data interpretation

Statistical analysis

Communication skills

Education

Bachelor/Master in science

Job description

AbbVie in Irvine, CA, is seeking a seasoned clinical trials professional to prepare scientific reports and manage data for multiple ongoing studies. The role focuses on drafting presentations, aligning protocols, and ensuring scientific integrity across studies.

You will coordinate advisory meetings, supervise project work, analyze PK, safety and efficacy data, and contribute to protocol development. A strong background in pharma clinical research and leadership is required, with hands-on