Product Safety Head (Sr Director) - Solid Tumors

Scorpion Therapeutics; Horsham (PA); On-site; USD 196,000 - 343,000; Full time

Job summary

Johnson & Johnson is seeking a Head of Product Safety for Solid Tumors based in the United States. You will oversee the medical safety strategy, lead Global Safety Officers and scientists, and drive risk management during drug development and post-marketing.

The role requires MD or equivalent with 10+ years in pharma, with emphasis on pharmacovigilance and oncology, and involves global regulatory interactions and cross-functional collaboration.

Qualifications

• MD or equivalent degree with clinical expertise and management experience.
• Expertise in pharmacovigilance, oncology products, and global regulatory guidelines.

Responsibilities

• Shape safety strategies for solid tumors and lead global safety officers and scientists.
• Manage regulatory submissions and responses and ensure compliance across regions.
• Collaborate with Medical Affairs, Regulatory, and other cross-functional teams.

Skills

Leadership

Strategic influence

Communication

Pharmacovigilance

Oncology safety

Regulatory planning

Education

MD or equivalent

Job description

Role:

Head of Product Safety for Solid Tumors at Johnson & Johnson, overseeing medical safety strategy and risk management during drug development and post-marketing.

Responsibilities:

• Responsibilities include shaping safety strategies, leading Global Safety Officers and scientists, managing regulatory submissions and responses, ensuring compliance, and collaborating with cross-functional teams such as Medical Affairs and Regulatory.
• The role entails proactive safety data assessment, safety profile evaluation, and communication with health authorities and stakeholders.
• The position involves global collaboration, leadership in regulatory interactions, and oversight of safety activities aligned with legal and regulatory standards.

Requirements:

• MD or equivalent with 10+ years pharma industry experience, clinical expertise, and management experience. Expertise in pharmacovigilance, oncology products, and global regulatory guidelines is essential, with a preference for oncology therapeutic area experience.

Skills:

• Skills include strong communication, leadership, and strategic influence, with knowledge of GxP, clinical trial conduct, and safety assessments.

Work setup and Compensation:

Work setup is based in Horsham, PA, Raritan, NJ, or Titusville, NJ. Salary range: $196K-$343K.