Manager, Medical Writing, Immunology

Johnson & Johnson Innovative Medicine; Spring House (PA); On-site; USD 140,000 - 200,000; Full time

Benefits offered by this job

None

Job summary

Johnson & Johnson's Innovative Medicine division is seeking a Manager, Medical Writing for Immunology to lead medical writing activities for clinical documentation in immunological disorders. The role involves preparing and finalizing documents, guiding cross-functional teams, mentoring staff, and ensuring regulatory compliance.

Remote work is considered on a case-by-case basis; based in Spring House, PA. You will set project objectives, drive process improvements, and serve as the program's

Qualifications

• Minimum 8 years in pharmaceutical or scientific fields; at least 6 years in medical writing.
• 2+ years of people management experience preferred.
• Strong communication, project management, and regulatory knowledge (ICH guidelines).

Responsibilities

• Prepare and finalize clinical documents.
• Lead or support cross-functional medical writing teams.
• Set project objectives.
• Mentor junior staff.
• Implement process improvements.
• Ensure compliance with industry and regulatory guidelines.
• Serve as primary contact for assigned programs, representing Medical Writing in cross-departmental and industry forums.

Skills

Medical Writing

Project Management

Regulatory Knowledge

People Management

Communication Skills

Education

Master's or PhD preferred

Job description

Role

Manager, Medical Writing for Immunology within Johnson & Johnson's Innovative Medicine division, leading medical writing activities for clinical documentation in the immunological disorders therapeutic area.

Responsibilities

• prepare and finalize clinical documents
• lead or support cross-functional medical writing teams
• set project objectives
• mentor junior staff
• implement process improvements
• ensure compliance with industry and regulatory guidelines.
• Serve as a primary contact for assigned programs, representing Medical Writing in cross-departmental and industry forums.

Requirements

• minimum 8 years of pharmaceutical or scientific experience, at least 6 years in medical writing, with a master's or PhD preferred
• 2+ years of people management experience preferred
• strong communication, project management, and regulatory knowledge (e.g., ICH guidelines).

High Value

• immunology
• clinical development
• regulatory medical writing
• team leadership
• cross-functional collaboration
• experience with complex clinical trial documentation

Work Setup

remote considered on a case-by-case basis; based in Spring House, PA.