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Live In Regulatory Medical Writer Jobs (NOW HIRING)

Significant experience in medical writing, particularly in regulatory submissions and clinical documentation * Strong understanding of regulatory requirements and industry standards for clinical ...

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

Lead Medical Writer Remote (must be based in EST) Compensation: $80-$90 per hour Contract Length: 2 ... Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred) * 5+ years of regulatory ...

Sr. Medical Writer (Regulatory) Syneos Health is a leading fully-integrated life sciences services ... Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you ...

About the Role We're looking for an experienced regulatory medical writer to act as our in-house pharma subject matter expert on a consulting basis. You'll work directly with our engineering team to ...

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

Medical Writing Manager

Salem, OR · Remote

$50 - $80/hr

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

Medical Writing Manager

Lowell, MA · Remote

$50 - $80/hr

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

Medical Writing Manager

Newark, NJ · Remote

$50 - $80/hr

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

Medical Writing Manager

Kent, WA · Remote

$50 - $80/hr

... regulatory writing in the context of AI. Preferred Qualifications * Minimum 5 years of regulatory ... medical writing experience at a sponsor, CRO, or as an independent consultant. * Direct experience ...

New

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Live In Regulatory Medical Writer information

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$14

$38

$57

How much do live in regulatory medical writer jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for live in regulatory medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is the difference between Live In Regulatory Medical Writer vs Regulatory Medical Writer?

AspectLive In Regulatory Medical WriterRegulatory Medical Writer
CredentialsTypically requires a life sciences degree and medical writing certificationSame as Live In role, often with additional regulatory training
Work EnvironmentUsually based at a single location, living on-site or nearbyOffice-based or remote, depending on employer
Employer & IndustryPharmaceutical, biotech companies, or CROsPharmaceutical, biotech, or regulatory agencies
Search & Comparison IntentOften searched by those seeking on-site or live-in rolesMore general, including remote or office roles

Live In Regulatory Medical Writers focus on on-site, live-in roles within pharmaceutical or biotech companies, requiring specific certifications and a preference for on-location work. Regulatory Medical Writers may work remotely or in-office, with similar qualifications, but without the live-in component. The main difference lies in the work setting and living arrangements.

What cities are hiring for Live In Regulatory Medical Writer jobs? Cities with the most Live In Regulatory Medical Writer job openings:
What are the most commonly searched types of Regulatory Medical Writer jobs? The most popular types of Regulatory Medical Writer jobs are:
What states have the most Live In Regulatory Medical Writer jobs? States with the most job openings for Live In Regulatory Medical Writer jobs include:

Principal Medical Writer

ICON

Blue Bell, PA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted yesterday


Job description

Principal Medical Writer
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information.
What You Will Do:
You will oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations.
Key responsibilities include:
  • Leading the preparation and review of clinical study reports, protocols, and other regulatory documents to ensure accuracy and clarity
  • Collaborating with cross-functional teams, including clinical research, biostatistics, and regulatory affairs, to gather and synthesize information for document development
  • Providing guidance on best practices for medical writing and ensuring adherence to regulatory requirements and internal standards
  • Mentoring and training junior medical writers, fostering a culture of excellence and professional growth
  • Staying current with industry trends and regulatory guidelines to inform writing practices and maintain high-quality outputs
  • Acting as a lead medical writer for complex projects and leading clinical/regulatory marketing approval applications for new biologics and drugs
  • The position includes all duties of a Senior Medical Writer, as well as leadership of regulatory approval application writing

Your Profile:
You will have solid experience in medical writing, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
  • A bachelor's degree in life sciences, pharmacy, or a related discipline
  • Significant experience in medical writing, particularly in regulatory submissions and clinical documentation
  • Strong understanding of regulatory requirements and industry standards for clinical writing
  • Exceptional writing and editing skills, with a keen eye for detail and clarity
  • Excellent communication and interpersonal skills, enabling effective collaboration with diverse teams and stakeholders

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply