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This job posting is for an Informed Consent Medical Writer at Merck, focusing on creating high-quality clinical and regulatory documents that support the company's development pipeline. The ideal candidate will have a background in health or life sciences, strong writing skills, and the ability to collaborate with cross-functional teams in a hybrid work environment.
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Job Summary
The Clinical and Regulatory Strategic Communications department creates and delivers high-quality regulated content in support of the development pipeline and enables data sharing for customers.
The Medical Writer will review accurate, clear, and compliant clinical, regulatory, and/or public-facing documents in support of the company portfolio.
The company offers a comprehensive package of benefits including medical, dental, vision, retirement benefits, paid holidays, vacation, and compassionate and sick days.
Matching Summary
Match Score: 75
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This job posting is for an Informed Consent Medical Writer at Merck, focusing on creating high-quality clinical and regulatory documents that support the company's development pipeline. The ideal candidate will have a background in health or life sciences, strong writing skills, and the ability to collaborate with cross-functional teams in a hybrid work environment.
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Salary
Base: $96,200.00 - $151,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, sick days
Skills & Requirements
Must-have
clinical regulatory documents
public-facing documents
health literacy principles
cross-functional teams
Microsoft Office Suite
Nice-to-have
plain language authoring
translating scientific content
company products understanding
emerging technology adaptation
Key Requirements
Bachelor's degree in health, scientific, or relevant discipline