Senior Scientific Director — Clinical Development Leader

BioSpace; Florham Park (NJ); On-site; USD 180,000 - 230,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

401(k) plan

Paid time off

Long-term incentive programs

Job summary

AbbVie in Florham Park, NJ is seeking a senior clinical development leader to oversee direction, planning and interpretation of clinical trials across programs. You will lead cross-functional teams to generate and disseminate high-quality data supporting product strategy.

The role requires in-depth knowledge of regulatory requirements, excellent English communication, and proven ability to manage complex, global clinical development programs with integrity and scientific rigor.

Qualifications

• Bachelor's degree in the sciences; advanced degree (e.g., MS, PhD) preferred.
• At least 8 years of relevant clinical trial experience in the pharmaceutical industry or equivalent.
• Ability to run a complex clinical research program independently.
• Proven leadership skills and ability to lead cross-functional global teams.
• Excellent English oral and written communication skills.

Responsibilities

• Leads the design and implementation of multiple clinical development programs.
• Oversees study teams and ensures enrollment and timelines for deliverables.
• Responsible for protocols, Investigator Brochures, Clinical Study Reports, and regulatory submissions.
• Acts as clinical lead and coordinates with internal stakeholders.
• Maintains compliance with Good Clinical Practices and regulatory requirements.
• Represents AbbVie at external meetings as needed.

Skills

Leadership

Cross-functional

English communication

Regulatory knowledge

Clinical development

Education

Bachelor's degree in sciences

MS or PhD preferred

Job description

AbbVie in Florham Park, NJ is seeking a senior clinical development leader to oversee direction, planning and interpretation of clinical trials across programs. You will lead cross-functional teams to generate and disseminate high-quality data supporting product strategy.

The role requires in-depth knowledge of regulatory requirements, excellent English communication, and proven ability to manage complex, global clinical development programs with integrity and scientific rigor.