Senior Medical Writer — Remote Lead, Clinical Documentation

LE1055 Perceptive Informatics, LLC

Massachusetts

Remote

USD 84,000 - 121,000

Full time

14 days+
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Benefits offered by this job

Health benefits
Paid time off
401(k) & insurance

Job summary

Perceptive Informatics, LLC is seeking a Senior Medical Writer for remote US-based work. You will create, research, edit and coordinate clinical documents related to independent review, serving as the client contact. The role focuses on information content authoring, project management and stakeholder engagement in regulated life sciences.

Proficiency with Microsoft Office and ICH-GCP is required. The annual base salary range is $84,368–$120,526, with benefits including health coverage, 401(k)

Qualifications

  • Bachelor's degree in science, pharmacy, nursing or health-related field or equivalent experience.
  • Fluent English (written and verbal).
  • Experience in regulated life sciences environments and with ICH-GCP guidelines.
  • Proficient in Microsoft Office (Word, Excel, PowerPoint).
  • Experience using data analysis tools such as Tableau or Power BI.

Responsibilities

  • Author, coordinate and finalize clinical documents for regulatory submission.
  • Serve as primary client contact for medical writing projects.
  • Ensure documents conform to SOPs and regulatory guidelines.
  • Conduct literature searches to support document development.
  • Review drafts and incorporate feedback from team members.
  • Develop and implement process improvements for documentation workflows.

Skills

Communication
Written communication
Stakeholder management
Attention to detail
Multitasking
Critical thinking
Microsoft Office
Agile
Life sciences knowledge

Education

Bachelor's Degree in a technical discipline

Tools

Tableau
Power BI

Job description

Perceptive Informatics, LLC is seeking a Senior Medical Writer for remote US-based work. You will create, research, edit and coordinate clinical documents related to independent review, serving as the client contact. The role focuses on information content authoring, project management and stakeholder engagement in regulated life sciences.

Proficiency with Microsoft Office and ICH-GCP is required. The annual base salary range is $84,368–$120,526, with benefits including health coverage, 401(k)

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