Oncology Clinical Development Director (Solid Tumors)

AbbVie; Massachusetts; On-site; USD 180,000 - 280,000; Full time

Job summary

AbbVie in Massachusetts is seeking a senior medical/clinical development professional to oversee design and execution of one or more clinical development programs, ensuring alignment with product strategy and regulatory requirements. The role requires an MD/DO, 2+ years of clinical trials experience, the ability to lead cross-functional teams, and strong English communication.

Collaboration with Medical Affairs, Clinical Operations, and Discovery will be essential to advance programs and

Qualifications

• MD/DO with relevant therapeutic specialty in an academic or hospital setting.
• At least 2 years of clinical trial experience in pharma, academia, or equivalent.
• Ability to run a clinical research program of moderate complexity with minimal supervision.
• Excellent oral and written English communication skills.
• Knowledge of clinical trial regulatory requirements and development of clinical strategy.

Responsibilities

• Design and oversee the conduct of one or more clinical development programs within a Product Development Plan.
• Oversee study integrity, safety data, enrollment timelines, and regulatory reporting.
• Design and interpret protocols, Investigator Brochures, Clinical Study Reports, and regulatory submissions.
• May oversee Medical Directors and Clinical Scientists on related programs.
• Provide in-house clinical expertise and collaborate with internal stakeholders.
• Stay current with literature and conferences to augment therapeutic area expertise.
• Ensure adherence to GCP, pharmacovigilance standards, and quality procedures.

Skills

Clinical trials

Leadership

English communication

Cross-functional collaboration

Education

MD or DO

Residency + subspecialty fellowship preferred

Job description

AbbVie in Massachusetts is seeking a senior medical/clinical development professional to oversee design and execution of one or more clinical development programs, ensuring alignment with product strategy and regulatory requirements. The role requires an MD/DO, 2+ years of clinical trials experience, the ability to lead cross-functional teams, and strong English communication.

Collaboration with Medical Affairs, Clinical Operations, and Discovery will be essential to advance programs and