Hematology Clinical Development Director

AbbVie; South San Francisco (CA); On-site; USD 180,000 - 280,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

401(k)

Long-term incentive programs

Paid time off

Job summary

AbbVie seeks a physician-lead to oversee clinical development programs, guiding cross-functional teams through study design, execution, and data interpretation. The role emphasizes safety, efficacy, and regulatory alignment across global trials.

The successful candidate has MD-level credentials, 2+ years in clinical trials, and strong English communication, with ability to manage complex programs and mentor junior staff.

Qualifications

• MD required with relevant therapeutic specialty (Oncology, Hematology).
• Minimum 2 years of clinical trial experience in pharma/academic settings.
• Ability to run a clinical research program of moderate complexity with minimal supervision.
• Ability to interact across a global cross-functional team to support strategy.
• Knowledge of clinical trial methodology and regulatory requirements.
• Excellent oral and written English communication skills.

Responsibilities

• Oversees design and execution of one or more clinical development programs.
• Monitors study integrity and data interpretation for safety and efficacy.
• Oversees enrollment timelines and reporting of adverse events per policy.
• Contributes to protocol design, regulatory submissions, and study reports.
• Provides in-house clinical expertise and participates in translational strategies as needed.
• May lead a Clinical Sub-team and coordinate with asset strategy teams.

Skills

Clinical trial management

Cross-functional collaboration

Regulatory/compliance knowledge

English communication

Leadership

Education

Medical Doctor (M.D.) or non-US equivalent

Job description

AbbVie seeks a physician-lead to oversee clinical development programs, guiding cross-functional teams through study design, execution, and data interpretation. The role emphasizes safety, efficacy, and regulatory alignment across global trials.

The successful candidate has MD-level credentials, 2+ years in clinical trials, and strong English communication, with ability to manage complex programs and mentor junior staff.