Senior Oncology Clinical Development Leader

Regulatory Jobs; Chicago (IL); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Benefits package

Long-term incentive programs

Paid time off

Job summary

AbbVie seeks a physician leader to oversee the direction, planning, execution, and interpretation of one or more clinical development programs. You will work with cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting product strategy.

The role involves designing and reporting protocols, Investigator Brochures, and regulatory submissions, while ensuring adherence to Good Clinical Practices and regulatory standards across studies.

Qualifications

• Minimum 2 years of clinical trial experience in pharma, academia, or equivalent.
• Excellent oral and written English communication skills.
• Knowledge of clinical trial methodology and regulatory requirements.

Responsibilities

• Oversees the direction, planning, execution, and interpretation of clinical trials.
• Oversees study enrollment timelines and data safety/efficacy reporting.
• Designs, analyzes, interprets, and reports scientific content of protocols and regulatory submissions.
• Provides clinical expertise and coordinates translational strategies with internal stakeholders.

Skills

Clinical trial experience

English communication

Regulatory knowledge

Education

MD/DO or non-US equivalent

Job description

AbbVie seeks a physician leader to oversee the direction, planning, execution, and interpretation of one or more clinical development programs. You will work with cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting product strategy.

The role involves designing and reporting protocols, Investigator Brochures, and regulatory submissions, while ensuring adherence to Good Clinical Practices and regulatory standards across studies.