Director, Clinical & Regulatory Communications Strategy

MSD; Pennsylvania; On-site; USD 173,000 - 273,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k) plan

Paid holidays

Sick days

Job summary

Merck & Co., Inc. is seeking a Director of Clinical and Regulatory Strategic Communications in Pennsylvania to lead, plan, and execute high-quality regulatory and public-facing documents across programs.

You will guide cross-functional teams, apply ICH GCP guidelines, and ensure compliance with regulatory standards. The role requires strategic collaboration with stakeholders across departments, mentorship of staff, and the ability to influence project timelines while maintaining scientific

Qualifications

• Bachelor's degree or higher in health, life sciences or related discipline.
• 7+ years in medical writing or industry experience.
• Experience leading complex clinical regulatory documents.
• Strong knowledge of ICH GCP and regulatory requirements.
• Excellent written and oral communication skills.

Responsibilities

• Lead design, planning, authoring, editing of regulatory and public-facing documents.
• Oversee multiple projects and teams to ensure timely delivery.
• Mentor and coach medical writers and cross-functional partners.
• Navigate regulatory requirements and industry guidelines to ensure compliance.

Skills

Medical Writing

Regulatory Compliance

Project Leadership

ICH GCP Guidelines

Regulatory Writing

Stakeholder Management

Education

Bachelor's degree or higher in health/science

Tools

Microsoft Office

SharePoint

Job description

Merck & Co., Inc. is seeking a Director of Clinical and Regulatory Strategic Communications in Pennsylvania to lead, plan, and execute high-quality regulatory and public-facing documents across programs.

You will guide cross-functional teams, apply ICH GCP guidelines, and ensure compliance with regulatory standards. The role requires strategic collaboration with stakeholders across departments, mentorship of staff, and the ability to influence project timelines while maintaining scientific