Senior Medical Writer: Clinical & Regulatory Strategy

MSD; Rahway (NJ); Vor Ort; USD 117.000 - 184.000; Vollzeit

Benefits dieser Stelle

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Paid holidays

Vacation

Sick days

Zusammenfassung

Merck & Co., Inc. in Rahway, NJ seeks an experienced Clinical and Regulatory Medical Writer to prepare regulatory and public-facing documents in alignment with regulatory requirements and health-literacy standards.

You will lead cross-functional teams, manage multiple projects, and ensure timely, compliant delivery of study reports, protocols, and participant materials. Strong communication and problem-solving skills are essential for success.

Qualifikationen

• Bachelor’s degree in a health, scientific, or relevant discipline and 3+ years of medical writing or industry experience.
• Experience managing multiple writing projects in a deadline-driven environment and leading teams of writers or cross-functional members.
• Strong oral and written communication and presentation skills; ability to interpret clinical data in line with regulatory requirements.
• Proficiency with common office tools (MS Office, SharePoint) and willingness to adopt new platforms.

Aufgaben

• Prepare clinical regulatory and/or public-facing documents per regulatory requirements.
• Lead cross-functional teams and manage workload to meet timelines and quality standards.
• Apply knowledge of medical writing best practices, industry guidelines, and data interpretation to produce high-quality documents.

Kenntnisse

Project management

Communication

Regulatory writing

Critical thinking

Negotiation

Team leadership

Ausbildung

Bachelor's degree in health/science

Tools

Microsoft Office

SharePoint

Jobbeschreibung

Merck & Co., Inc. in Rahway, NJ seeks an experienced Clinical and Regulatory Medical Writer to prepare regulatory and public-facing documents in alignment with regulatory requirements and health-literacy standards.

You will lead cross-functional teams, manage multiple projects, and ensure timely, compliant delivery of study reports, protocols, and participant materials. Strong communication and problem-solving skills are essential for success.