Senior Aesthetics Clinical Development Lead

BioSpace; Irvine (CA); On-site; USD 120,000 - 170,000; Full time

Benefits offered by this job

Health benefits

401(k) plan

Long-term incentives

Paid time off

Job summary

AbbVie in Irvine, CA is seeking an experienced clinical data professional to build data and information for internal clinical trial documents and reports, coordinating multi-task efforts to keep studies moving forward. You will contribute to protocols, study development, and data interpretation with rigor and scientific integrity.

The role demands strong statistical thinking, advanced reporting skills, and ability to lead cross-functional teams while delivering high-quality presentations and

Qualifications

• Bachelor’s or Master’s in Science with 11+ years in pharma.
• PharmD or PhD with relevant clinical trial experience.
• Ability to interpret clinical study data and create presentations.
• Experience supporting drug development and study leadership.
• Strong communication and project management skills.

Responsibilities

• Prepare scientific reports/presentations for clinical trials using templates.
• Coordinate advisory meeting agendas, slide decks and consulting agreements.
• Comply with IQS procedures and study protocols issued by management.
• Lead study development with electronic document conventions to ensure integrity.
• Receive tasks from function/MD and meet timelines with minimal supervision.
• Participate in process improvement initiatives affecting timelines.
• Analyze study data including PK, safety and efficacy using statistics software.
• Perform literature searches to resolve problems with current document conventions.
• Present key study information to management and therapeutic area leads.
• May lead teams and mentor personnel within the therapeutic area.

Skills

Clinical data analysis

Scientific reporting

Cross-functional leadership

Presentation skills

Communication

Education

Bachelor’s/Master’s in Science

PharmD/PhD

Tools

SAS

Tableau

R

Job description

AbbVie in Irvine, CA is seeking an experienced clinical data professional to build data and information for internal clinical trial documents and reports, coordinating multi-task efforts to keep studies moving forward. You will contribute to protocols, study development, and data interpretation with rigor and scientific integrity.

The role demands strong statistical thinking, advanced reporting skills, and ability to lead cross-functional teams while delivering high-quality presentations and