Informed Consent Medical Writer

Muckelab

Base: $96,200.00 - $151,400.00; bonus/equity: elig...
Hybrid (3 days onsite, 1 day remote)
Health literacy principles
Clinical regulatory documents
Plain language summaries
Muckelab is seeking an Informed Consent Medical Writer to join their Clinical and Regulatory Strategic Communications department. The role requires expertise in medical writing, collaboration with cross-functional teams, and adherence to regulatory standards while creating clear, compliant documents

Job Summary

  • The Clinical and Regulatory Strategic Communications department creates and delivers high-quality regulated content and enables data sharing, ensuring excellence and compliance while incorporating health literacy principles.
  • The Medical Writer will author, edit, and review accurate, clear, and compliant clinical, regulatory, and public-facing documents, demonstrating growing competence and independence.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement, paid holidays, and vacation.

Matching Summary

Match Score: 85

Muckelab is seeking an Informed Consent Medical Writer to join their Clinical and Regulatory Strategic Communications department. The role requires expertise in medical writing, collaboration with cross-functional teams, and adherence to regulatory standards while creating clear, compliant documents.

Salary

Base: $96,200.00 - $151,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • Health literacy principles
  • Clinical regulatory documents
  • Plain language summaries
  • Cross-functional teams
  • Stakeholder collaboration

Nice-to-have

  • Adaptability and problem-solving
  • Keenness to learn new technology
  • Inclusive and diverse environment
  • Critical evaluation of data

Key Requirements

  • Bachelor's degree in health, scientific, or relevant discipline
  • At least 2 years of relevant industry experience
  • Knowledge of clinical research principles
  • Strong attention to detail and analytical skills
  • Ability to manage multiple projects
  • Strong oral and written communication skills
  • Technical expertise in office applications and shared document systems

Work Rights

Not specified

Tailored Resume

Cover Letter