Senior Medical Director — Oncology Clinical Development

AbbVie; Florham Park (NJ); On-site; USD 150,000 - 210,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Long-term incentive programs

Job summary

AbbVie in Florham Park, NJ seeks a clinical development professional to oversee direction, planning, execution and interpretation of clinical trials within a development program. Under supervision, you will contribute to high-quality data supporting product strategy.

You will design study protocols, monitor study integrity, assess safety and efficacy data, and collaborate across Medical Affairs, Clinical Operations and other functions to advance development plans and regulatory readiness.

Qualifications

• Ability to run a clinical research study with appropriate supervision.
• Strong collaboration in a cross-functional setting.
• Experience with clinical trials in pharma, academia, or equivalent.
• Knowledge of trial methodology, regulatory and compliance requirements.

Responsibilities

• Oversees design and implementation of study protocols for a clinical development program.
• Monitors study integrity and safety/efficacy data.
• Contributes to regulatory submissions and clinical study reports.
• Collaborates with Medical Affairs, Commercial and other functions as required.

Skills

Cross-functional collaboration

English communication

Clinical trial experience

Regulatory awareness

Study protocol design

Education

MD/DO or equivalent

Residency completed

Fellowship desirable

Job description

AbbVie in Florham Park, NJ seeks a clinical development professional to oversee direction, planning, execution and interpretation of clinical trials within a development program. Under supervision, you will contribute to high-quality data supporting product strategy.

You will design study protocols, monitor study integrity, assess safety and efficacy data, and collaborate across Medical Affairs, Clinical Operations and other functions to advance development plans and regulatory readiness.