New · posted Nov 1
ICON · Pharmaceuticals
Principal Medical Writer
- Blue Bell, PA
- On-site
- Full-time
- Senior & Principal
The role
Principal Medical Writer
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
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 need
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.
What you'll 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
Pay and benefits
ICON didn't publish pay for this role
See what similar roles pay on Regulatory Jobs, or try the salary calculator.
Rewards & Benefits
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
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Where you'll work
Blue Bell, PAOn-siteOpen in Maps (opens in a new tab)
More jobs in Blue Bell, PAEqual opportunity, accessibility and legal noticesICON's statements, word for word
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
Job intelligence
The context around this role
Live data · November 1, 2026
Salary intelligence
How the pay compares
Senior & Principal roles in the US12 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $131,125 | $146,000 | $178,500 |
Comparisons: the base pay employers published on open Clinical Evaluation & Medical Writing roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Evaluation & Medical Writing
The general path across 39 open Clinical Evaluation & Medical Writing roles on Regulatory Jobs, with the titles they carry most. Not ICON's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 21 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs11
- Collaboration and leadership8
- Clinical trial conduct2
- Lab testing and methods1
- Regulatory submissions1
Company hiring pulse
ICON on Regulatory Jobs
- 106
- Open roles
- 56
- Distinct roles
- 30
- Locations
By discipline
- Clinical96 91%
- Quality7 7%
- Regulatory3 3%
By level
- Senior & Principal45 42%
- Associate & Specialist43 41%
- Manager15 14%
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Principal Medical Writer at ICON
Open until filled.