Global Study Feasibility Director

Allergan; South San Francisco (CA); On-site; USD 180,000 - 230,000; Full time

Benefits offered by this job

PTO

Medical/Dental/Vision Insurance

401(k)

Job summary

AbbVie in South San Francisco, CA seeks an Study Feasibility Associate Director to partner with study teams on design feasibility and recruitment timelines. You will influence strategy, review protocols, and optimize execution while managing global studies.

This role emphasizes collaboration, analytics, and leadership within Clinical Development Operations. You will leverage extensive clinical study design experience and operate across oncology, neurology, or immunology programs, guiding complex

Qualifications

• Minimum 8 years in pharma with 5+ years in clinical research/leadership.
• Degree in pure, applied, or technical sciences preferred.
• Drug development and/or scientific project leadership experience preferred.
• Therapeutic area background in Oncology, Neurology, or Immunology preferred.
• Strong working knowledge of pharma drug development processes.

Responsibilities

• Designs and facilitates cross-functional strategy discussions with AbbVie leaders to assess feasibility.
• Supports global phase 2/3 trial delivery with large-scale international studies.
• Matrix-manages to drive insights and recruitment planning across teams.
• Conducts detailed scientific, analytical, and operational analyses for study teams.
• Provides consultation on country strategy, site selection, and timelines.
• Leads projects to improve Study Feasibility & Recruitment capabilities.

Skills

Cross-functional leadership

Facilitation skills

Study design

Operations management

Education

Bachelor’s or advanced Degree in sciences

Job description

AbbVie in South San Francisco, CA seeks an Study Feasibility Associate Director to partner with study teams on design feasibility and recruitment timelines. You will influence strategy, review protocols, and optimize execution while managing global studies.

This role emphasizes collaboration, analytics, and leadership within Clinical Development Operations. You will leverage extensive clinical study design experience and operate across oncology, neurology, or immunology programs, guiding complex