Hybrid Associate Director, Global Clinical Development

Biopharma Careers; United States; Hybrid; USD 150,000 - 210,000; Full time

Benefits offered by this job

Vacation & holidays

Medical/dental/vision insurance

401(k) plan

Long-term incentives

Job summary

AbbVie is seeking an Associate Director of Clinical Development based in Irvine, CA with a hybrid schedule (3 days in office). The role designs, develops, and executes clinical studies, providing medical direction to multi-disciplinary teams and ensuring rigorous data interpretation within regulatory standards.

The candidate will mentor staff, contribute to process improvements, and lead cross-functional activities across medical affairs, statistics, regulatory, and clinical operations to

Qualifications

• Advanced degree in a relevant field (MD/DO/PhD/PharmD) preferred.
• 7+ years of Clinical Development experience.
• Experience with regulatory submissions and global/regulatory interactions.
• Strong English communication and leadership skills.

Responsibilities

• Design and execute clinical trials within the Product Development Plan.
• Provide scientific direction to project teams and mentor junior members.
• Lead cross-functional collaborations with medical affairs, regulatory, and operations.
• Ensure data integrity and regulatory compliance.

Skills

Clinical Development

Cross-functional collaboration

Regulatory knowledge

Education

MD/DO/PhD/PharmD

Job description

AbbVie is seeking an Associate Director of Clinical Development based in Irvine, CA with a hybrid schedule (3 days in office). The role designs, develops, and executes clinical studies, providing medical direction to multi-disciplinary teams and ensuring rigorous data interpretation within regulatory standards.

The candidate will mentor staff, contribute to process improvements, and lead cross-functional activities across medical affairs, statistics, regulatory, and clinical operations to