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Clinical Writer Jobs (NOW HIRING)

ICON

Principal Medical Writer

Blue Bell, PA · On-site +1

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 ...

Icon plc

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 ...

Laborie

Medical Writer II

Mechanicsburg, PA · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Laborie

Medical Writer II

Plymouth, MN · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Laborie

Medical Writer II

Minnetonka, MN · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Laborie

Medical Writer II

Westborough, MA · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Laborie

Medical Writer II

Orangeburg, NY · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Laborie

Medical Writer II

Portsmouth, NH · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

Laborie

Medical Writer II

Salt Lake City, UT · Hybrid

$115K - $125K/yr

The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents and presentations for internal support, global regulatory agencies, and ...

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Clinical Writer information

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$25

$54

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How much do clinical writer jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for clinical writer in the United States is $54.35, according to ZipRecruiter salary data. Most workers in this role earn between $39.90 and $64.18 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Writer, and why are they important?

To thrive as a Clinical Writer, you need a solid background in life sciences or medical fields, excellent writing skills, and attention to detail, often supported by a relevant degree. Familiarity with regulatory guidelines, literature databases, and tools like EndNote, as well as certifications such as AMWA or EMWA, are highly valued. Strong communication, critical thinking, and time management help Clinical Writers convey complex information clearly and collaborate with medical professionals. These skills ensure the accuracy, clarity, and compliance of clinical documents critical for regulatory submissions and advancing medical knowledge.

What does a clinical writer do?

A clinical writer creates scientific and regulatory documents for healthcare and pharmaceutical industries, such as clinical study reports, protocols, and regulatory submissions. They ensure accuracy, clarity, and compliance with industry standards, often working with data from clinical trials and using tools like Microsoft Word and reference management software.

How much do medical writers make a month?

Medical writers, including clinical writers, typically earn between $4,000 and $8,000 per month depending on experience, education, and location. Entry-level positions may start lower, while experienced professionals with specialized skills or certifications can earn higher salaries, especially in biotech or pharmaceutical industries.

Is there a demand for medical writers?

There is strong demand for clinical writers, especially those with expertise in regulatory writing, medical communications, and scientific documentation. The healthcare and pharmaceutical industries regularly seek qualified medical writers to produce clinical trial reports, regulatory submissions, and scientific publications, often requiring familiarity with tools like Microsoft Word and industry guidelines such as ICH and GCP.

What kind of jobs in media bring in $150,000 a year?

High-paying media jobs that can reach $150,000 annually include senior roles such as media directors, executive producers, and content strategists, often requiring extensive experience, leadership skills, and industry knowledge. Positions in digital media, advertising, and broadcasting that involve management or specialized expertise tend to offer higher salaries, especially in larger organizations or with advanced certifications.

What is a Clinical Writer?

A Clinical Writer is a professional who creates, edits, and manages medical and scientific documents related to clinical research, healthcare, and pharmaceuticals. They often prepare clinical study reports, regulatory submissions, patient information leaflets, and scientific manuscripts. Clinical Writers work closely with researchers, physicians, and regulatory professionals to ensure that complex clinical information is communicated clearly, accurately, and in compliance with industry standards. Their work is essential for documenting clinical trials and supporting the approval of new drugs or therapies.

What are some common challenges clinical writers face when translating complex medical research into accessible documents?

Clinical writers often encounter the challenge of interpreting highly technical and data-rich research while ensuring accuracy and regulatory compliance. Balancing the need for scientific precision with the ability to communicate information clearly to various audiences—such as healthcare professionals, regulatory agencies, or patients—requires strong analytical and communication skills. Additionally, clinical writers must stay updated on evolving guidelines and collaborate closely with subject matter experts, which can be demanding but also enriches their expertise and professional network.
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Clinical Writer jobs near you
Infographic showing various Clinical Writer job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 3% As Needed, 69% Full Time, 18% Part Time, and 9% Contract. Highlights an 54% Physical, 2% Hybrid, and 44% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.
Principal Medical Writer

Principal Medical Writer

ICON

Blue Bell, PA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 7 days ago

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

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