MD – Oncology Clinical Development Lead

AbbVie Inc.; Florham Park (NJ); On-site; USD 140,000 - 210,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k) program

Job summary

AbbVie is seeking a physician leader to oversee direction, planning, and interpretation of clinical trials within a development program. You will participate in cross-functional teams to deliver high-quality clinical data supporting product strategy.

With supervision, you will ensure study design, enrollment timelines, and safety/efficacy data interpretation align with regulatory requirements. You will contribute to study reports and regulatory submissions and stay current with scientific

Qualifications

• Must have clinical trial experience in pharma, academia, or equivalent.
• Ability to run a clinical research study with appropriate supervision.
• Strong desire to collaborate in a cross-functional setting.
• Excellent oral and written English communication skills.
• Knowledge of clinical trial methodology and regulatory requirements.

Responsibilities

• Oversees design and implementation of study protocols within a development program.
• Monitors study integrity and data interpretation for safety and efficacy.
• Supports Regulatory submissions and clinical study reports with scientific content.
• Participates in cross-functional Clinical Strategy Team discussions.
• Stays current with developments by attending conferences and reviewing literature.
• Ensures adherence to Good Clinical Practices and quality standards.

Skills

Clinical trial experience

Cross-functional collaboration

English communication

Education

MD/DO or non-US equivalent

Job description

AbbVie is seeking a physician leader to oversee direction, planning, and interpretation of clinical trials within a development program. You will participate in cross-functional teams to deliver high-quality clinical data supporting product strategy.

With supervision, you will ensure study design, enrollment timelines, and safety/efficacy data interpretation align with regulatory requirements. You will contribute to study reports and regulatory submissions and stay current with scientific