Senior Clinical Development Director

Allergan; South San Francisco (CA); On-site; USD 150,000 - 210,000; Full time

Job summary

AbbVie is seeking an experienced clinical development leader to guide multi-program strategies and deliver high-quality data. You will oversee study design, enrollment, timelines and regulatory submissions while coordinating with medical affairs, operations and other functions.

Strong English communication and global collaboration are essential for success. In this role you will supervise scientific directors and contribute to integrated evidence plans, ensuring alignment with regulatory

Qualifications

• Bachelor's degree in the sciences; advanced degree (MS/PhD/PharmD) preferred.
• 5+ years of clinical trial experience in pharma, academia, or equivalent.
• Ability to lead clinical study programs with limited supervision.
• Strong cross-functional collaboration and external stakeholder interaction.
• In-depth knowledge of regulatory requirements and compliance.
• Excellent oral and written English communication skills.

Responsibilities

• Leads design, planning and interpretation of clinical development programs.
• Oversees study enrollment, timelines, and data integrity across programs.
• Responsible for protocols, regulatory submissions and study reports.
• May supervise Medical Directors and Clinical Scientists on related programs.
• Contributes to Integrated Evidence Strategy and cross-functional plans.
• Represents clinical development in regulatory discussions and external meetings.

Skills

Clinical trial leadership

Regulatory knowledge

Cross-functional collaboration

English communication

Education

Bachelor's degree in sciences

Advanced degree preferred

Job description

AbbVie is seeking an experienced clinical development leader to guide multi-program strategies and deliver high-quality data. You will oversee study design, enrollment, timelines and regulatory submissions while coordinating with medical affairs, operations and other functions.

Strong English communication and global collaboration are essential for success. In this role you will supervise scientific directors and contribute to integrated evidence plans, ensuring alignment with regulatory