Senior Medical Writer & Regulatory Content Lead

MSD International; North Wales (Montgomery County); Presencial; USD 142.000 - 224.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Dental insurance

Vision insurance

401(k) plan

Paid holidays

Vacation

Sick days

Descripción de la vacante

Merck & Co., Inc. in USA is seeking a Principal Medical Writer to lead the authoring, editing, and review of regulatory and clinical documents across multiple programs.

You will partner with a project lead to ensure accuracy, compliance, and clear, audience-appropriate communications. The role requires 5+ years in medical writing, a health/science degree, and strong leadership, collaboration, and problem-solving skills.

Formación

• Bachelor’s degree or higher in health, science or related field.
• 5+ years of medical writing or industry experience.

Responsabilidades

• Lead design, authoring, editing and reviewing regulatory/clinical documents.
• Collaborate with cross-functional teams and manage project timelines.
• Mentor and coach other medical writers.
• Ensure compliance with regulatory requirements and health literacy standards.

Conocimientos

Medical writing

Regulatory knowledge

Leadership

Critical thinking

Communication

MS Office

Educación

Bachelor’s degree or higher

Herramientas

Microsoft Office Suite

SharePoint

Descripción del empleo

Merck & Co., Inc. in USA is seeking a Principal Medical Writer to lead the authoring, editing, and review of regulatory and clinical documents across multiple programs.

You will partner with a project lead to ensure accuracy, compliance, and clear, audience-appropriate communications. The role requires 5+ years in medical writing, a health/science degree, and strong leadership, collaboration, and problem-solving skills.