Aesthetics Clinical Development Lead

Regulatory Jobs; Irvine (CA); On-site; USD 150,000 - 210,000; Full time

Job summary

AbbVie seeks a seasoned professional to prepare scientific reports for clinical trials, review protocols, and ensure data integrity across studies. You will lead documentation and contribute to presentations, with emphasis on accuracy and regulatory alignment.

The role requires advanced degrees in science and substantial experience in pharmaceutical research, with strong communication and project leadership skills. On-site in Irvine, CA.

Qualifications

• Bachelor's/Master’s degree in Science or related field.
• PharmD/PhD with 1+ year in pharma or related field.
• Ability to analyze clinical study data and generate reports.

Responsibilities

• Prepare scientific reports/presentations for clinical trials using standard templates.
• Coordinate advisory meeting agendas, activities and slide decks.
• Ensure compliance with IQS and study protocols; manage timelines.

Skills

Scientific reporting

Data interpretation

Literature searches

Team collaboration

Education

Bachelor's/Master's in Science

PharmD/PhD with 1+ year

Job description

AbbVie seeks a seasoned professional to prepare scientific reports for clinical trials, review protocols, and ensure data integrity across studies. You will lead documentation and contribute to presentations, with emphasis on accuracy and regulatory alignment.

The role requires advanced degrees in science and substantial experience in pharmaceutical research, with strong communication and project leadership skills. On-site in Irvine, CA.