Senior Medical Writer & Regulatory Strategy Lead

Merck & Co.; Rahway (NJ); On-site; USD 142,000 - 224,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Medical, dental, vision benefits

Job summary

Merck & Co. in Rahway, NJ, seeks a Principal Medical Writer within Global Clinical Trial Operations to develop, edit, and lead compliant clinical and regulatory documents for multiple programs. You will partner with project leads to ensure timely delivery, scientific excellence, and cross-functional collaboration.

The role requires advanced medical writing expertise, leadership capabilities, and a commitment to health literacy and regulatory standards in a dynamic environment.

Qualifications

• Bachelor's degree or higher in health/science field.

Responsibilities

• Lead the design, authoring, editing, and review of clinical, regulatory, and public-facing documents across programs.

Job description

Merck & Co. in Rahway, NJ, seeks a Principal Medical Writer within Global Clinical Trial Operations to develop, edit, and lead compliant clinical and regulatory documents for multiple programs. You will partner with project leads to ensure timely delivery, scientific excellence, and cross-functional collaboration.

The role requires advanced medical writing expertise, leadership capabilities, and a commitment to health literacy and regulatory standards in a dynamic environment.